Class 11 Chapter 9 Chemistry Competency Based Question Bank With
Class 11 Chapter 9 Chemistry Competency Based Question Bank With
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a) b) c) d)
a)
b)
c)
d)
a) b)
a) b) c) d)
32. 400−600℃
CH3 CH2 CH3 → 𝑋 + 𝑌, 𝑋 and 𝑌 are
a) Hydrogen and methane b) Hydrogen and ethylene
c) Ethylene and methane d) Any of these
33. Position of double bond in alkenes is identified by
a) Ozonolysis b) Bromine water
c) Ammonical silver nitrate d) None of these
34. Consider the following reaction
I. H2 /Ni2 B
II. H2 /Pd − CaCO3 in quinoline
III. Na/NH3 or LiAIH4
This reaction takes place by
a) I or II b) I or III c) II or III d) I, II or III
35. Which of the following reagent can distinguish between 1-butyne and 2-butyne?
a) Aqueous NaOH
b) Bromine water
c) Fehling’s solution
d) AmmoniacalAgNO3
36. CH4 is formed when:
a) Sodium acetate is heated with soda lime
b) Iodo methane is reduced
c) Aluminium carbide reacts with water
d) All of the above
37. Reaction of HBr with propene in the presence of peroxide gives
a) 𝑖𝑠𝑜-propyl bromide b) 3-bromo propane c) Allyl bromide d) 𝑛-propyl bromide
38. Predict structure of 𝑋 in following reaction
a) b) c) d)
a) Eglinton’s reaction
b) Glaser reaction
c) Gomberg-Beckmann’s reaction
d) Leuckart reaction
49. 2-Hexyne gives 𝑡𝑟𝑎𝑛𝑠-2-hexene on treatment with:
a) Li/NH3 b) Pd/BaSO4 c) LiAlH4 d) Pt/H2
50. Which of the following will give three mono-bromo derivatives?
a) CH3 CH2 CH2 CH(CH3 )CH3 b) CH3 CH2 C(CH3 )2 CH3
c) CH3 CH3 (CH3 )CH (CH3 )CH3 d) All the above can give
51. The reagent for the following conversion
a) b) c) d)
a) b) c) d)
a) b)
a)
b)
c)
d)
on ozonolysis gives
d) None of these
a) b) c)
is non-aromatic.
c) The hybrid state of carbon in carbonyl group is 𝑠𝑝2 .
d) The hyperconjugative effect is known as no bond resonance.
120. An alkene on vigorous oxidation with KMnO4 gives only acetic acid. The alkene is
a) CH3 CH2 CH = CH2 b) CH3 CH = CHCH3 c) (CH3 )2 C = CH2 d) CH3 CH = CH2
121. A hydrocarbon reacts with hypochlorous acid to give 2-chloroethanol. The hydrocarbon is:
a) Methane b) Ethylene c) Acetylene d) Ethane
122. The angle strain in cyclobutane is
a) 24°44′ b) 29°16′ c) 19°22′ d) 9°44′
123. During chlorination of methane usually a mixture of all the chlorinated products, 𝑖. 𝑒., methyl chloride,
methylene dichloride, chloroform and carbon tetrachloride are obtained. What will happen, if we use
excess of Cl2 in this reaction?
a) Only methyl chloride will be formed
b) Only chloroform will be formed
c) Only CCl4 will be formed
d) Only methylene dichloride will be formed
124. Aromatization of 𝑛-heptane and 𝑛-octane gives respectively:
a) Toluene, ethyl benzene
b) Ethyl benzene, toluene
c) Toluene, benzene
d) Benzene, ethyl benzene
125. Which of the following organic compounds exhibit acidic character?
a) H3 C − C ≡ CH b) H3 C − C ≡ C − CH3 c) H2 C = CH2 d) H3 C − CH3
126. Sodium formate on heating with soda lime gives:
a) CH4 b) CO2 c) H2 d) All of these
127. Which of the following can be used for preparation of propane?
1.B2H6 1.Mg/ether
a) CH3 CH = CH2 → b) CH3 CH2 CH2 Cl →
2.AgNO3/NaOH 2.H2O2
HI/∆ 150℃ NaOH(CuO)
c) CH3 CH2 CH2 I → d) CH3 CH2 CH2 COONa →
∆
128. The marsh gas detector used by miners works on the principle of:
a) Difference in the rates of diffusion of gases
b) Avogadro’s hypothesis
c) Gay-Lussac’s law of gaseous volumes
d) Berzelius hypothesis
129. The compound with highest boiling point.
a) 𝑛-nexane b) 𝑛-pentene
c) 2,2-dimethyl propane d) 2-methyl butane
130. The most stable conformation of chlorocyclohexane at room temperature is:
a) b) c) d)
a) b)
c) d)
a) b)
c) d)
147.
a) b) c) d)
a)
b)
c)
a)
b)
c)
d)
154. Which of the following reagents when heated with ethyl chloride, forms ethylene?
a) Aqueous KOH b) Zn⁄HCl c) Alcoholic KOH d) HI
155. Reduction of 2-methyl-1-bromopropane with metal and acid gives:
a) Butyl bromide b) 𝑛-butane c) Isobutene d) None of these
156. Dehydration of 2-butanol yield
a) 1-butene b) 2-butene c) 2-butyne d) Both (a) and (b)
157. Which statement is correct?
a) Knocking decreases the efficiency of an internal combustion engine
b) Knocking cannot be eliminated completely by adding anti-knock compounds
c) The higher the octane number, the better is the quality of fuel
d) All of the above
158.
The treatment of with NaIO4 or boiling KMnO4 produces
KMnO4 produces
a) CH3 COCH3 + CH3 COOH b) CH3 COCH3 + CH3 CHO
c) CH3 CHO + CO2 d) CH3 COCH3 only
159. Which of the following reagents will be able to distinguish between 1-butyne and 2-butyne?
a) NaNH2 b) HCl c) O2 d) Br2
160. 2-chloro-3-methylbutane is treated with sodium in etherial solution, then it will give
a) 2,4-dimethylhexane b) 3,5-dimethylhexane
c) 2,3,4,5-tetramethylhexane d) 2,6-dimethyloctane
161. The hydrocarbon which can react with sodium in liquid ammonia is
a) CH3 CH2 CH2 C ≡ CCH2 CH2 CH3 b) CH3 CH2 C ≡ CH
c) CH3 CH = CHCH3 d) CH3 CH2 C ≡ CCH2 CH3
162. Which of the following is incorrect? The members of the homologous series of alkanes?
a) Are all straight chain compounds
b) Have the general formula C𝑛 H2𝑛+2
c) Show a regular gradation in physical properties
d) Have similar chemical properties
163. Ammoniacal cuprous chloride will give red precipitate with which one of the following?
a) CH3 − C ≡ C − CH3 b) CH3 − CH = CH2
c) CH3 − C ≡ CH d) CH3 − CH = CH − CH3
164. Mustard gas is:
a) CH4 b) C2 H4 c) CH2 Cl— CH2 — S— CH2 —d)CHNone
2 Cl of the above
165. During pyrolysis of alkane, C—C bond rather than C—H bond break because:
a) C—C bond is reactive site in alkane
b) C—H bond is reactive site in alkane
c) Bond energy of C—C is lower than C—H bond
d) Energy of activation of C—C bond is very high
166. A mixture of CH4 and steam on passing over nickel suspension on alumina at 800° C gives:
a) CO only b) H2 only c) CO and H2 d) None of these
167. A compound 𝑋(C5 H8 ) reacts with ammoniacalAgNO3 to give a white precipitate, and on oxidation with hot
alkaline KMnO4 gives the acid,(CH3 )2 CHCOOH. Therefore, 𝑋 is
a) CH2 = CHCH = CHCH3 b) CH3 (CH2 )2 C ≡ CH c) (CH3 )2 CH − C ≡ CH d) (CH3 )2 C = C = CH2
168. What are the products obtained by the ozonolysisof𝑅CH = C𝑅1 𝑅2 ?
a) 𝑅1 CH2 CH2 𝑅2 b) 𝑅2 CO c) 𝑅1 CO𝑅2 d) None of these
169. Following compound is treated with NBS
Compound formed A is
a) b)
c) d)
170. The structural formula of the compound which yields ethylene upon reaction with zinc:
a) CH2 Br— CH2 Br b) CHBr2 — CHBr2 c) CHBr=CHBr d) None of these
171. An alkyne combines with a conjugated diene to give an unconjugatedcycloalkadiene. The most
likely title of this reaction is
a) Schotten-Baumann reaction b) Hofmann-bromamide reaction
c) Pinacol-Pinacolone rearrangement d) Deils-Alder reaction
172. The most important method of preparation of hydrocarbons of lower carbon number is:
a) Pyrolysis of higher carbon number hydrocarbons
b) Electrolysis of salts of fatty acids
c) Sabatier-Senderen’s reaction
d) Direct synthesis
173. The number of carbon atoms in hydrocarbons of kerosene is in the range of:
a) C5 — C7 b) C12 — C16 c) C1 — C4 d) C17 — C20
174. A mixture of 1-chlorobutane and 2-chlorobutane when treated with alcoholic KOH gives
a) 1-butene b) 2-butene
c) 𝑖𝑠𝑜-butylene d) Mixture of 1-butene+2-butene
175. Which of the following react with Cl2 and Br2 at room temperature and in the absence of diffused sunlight
to produce dihalogen derivatives?
a) Cyclobutane b) Cyclopentane c) Cyclohexane d) All of these
176. A compound (X) on ozonolysis followed by reduction gives an aldehydeC2 H4 O and 2-butanone,
compound (X) is
a) 3-methyl pentene-2 b) 3-methyl pentene-3 c) 3-methyl hexene-3 d) 3-ethyl pentene-3
177. An octane number 100 is given to:
a) 𝑛-hexane b) Iso-octane c) Neopentane d) Neo-octane
178. When butene-1 is mixed with HBr, the major reaction product is:
a) 1,2-dibromobutane b) 1-bromobutane c) 2-bromobutane d) None of these
179. Which cycloalkane has the lowest heat of combustion per CH2 group?
a) Cyclopropane b) Cyclobutane c) Cyclopentane d) Cyclohexane
180. The order of appearance of the following with rising temperature during the refining of crude oil is:
a) Kerosene, gasoline, diesel
b) Diesel, gasoline, kerosene
c) Gasoline, diesel, kerosene
d) Gasoline, kerosene, diesel
181. CH — C ≡ C— CH NaNH2
𝑋; what is X ?
3 3→
182.
A(Predominantly) is:
a)
b)
c)
d)
a)
b)
c)
is:
a) The same b) (A)>(B)>(C) c) (A)<(B)<(C) d) (A)>(B)=(C)
194. Action of 𝑅Mg X with vinyl chloride gives:
a) Alkane b) Alkyne c) Alkene d) All of these
195. The following reaction is called
a) b) c) d)
204. During Wurtz reaction, which of the following is sometimes also obtained because of decomposition of
free radicals?
a) Alkynes b) Alkenes c) CO2 d) Alkyl halide
205. Which of the following reagents cannot be used to locate the position of triple bond in CH3 — C ≡ C— CH3 ?
a) Br2 b) O3 c) Cu+ d) KMnO4
206. Decarboxylation of malonic acid gives:
a) CH4 b) C2 H6 c) C3 H8 d) None of these
207.
a) b) c) d)
a) b) c)
a) b) c) d)
254. The treatment of ethane with cold alkaline potassium permanganate produces
a) Ethylene glycol b) Formaldehyde
c) Formic acid d) Carbon dioxide and water
255. As compared to melting points of even carbon chain isomers, the melting points of odd carbon chain
alkanes are:
a) Lower
b) Higher
c) Same
d) Not depend upon branching
256. Hg2+ /H+
Ph − C ≡ C − CH3 → 𝐴,
a) b) c) d)
a) b) c) d) CH3 C ≡ CH = CH2
a) b) c) d)
a) b) c) d)
291. Addition of hydrogen on C=C is called hydrogenation. Addition of halogen on C=C is called:
a) Halogenation
b) Dehalogenation
c) Elimination of halogen
d) None of these
292. The synthetic gas is:
a) CH4 b) C2 H2 c) CO + 3H2 d) NH3
293. Toluene on treatment with CrO3 and (CH3 CO)2 O followed by hydrolysis with dil. HCl gives
a) Benzaldehyde b) Benzoic acid c) Phenol d) Phenylacetaldehyde
294. Identify the product (P) in the reaction:
Alk.KMnO4
𝑅3 C— H → P
a) No reaction b) 𝑅3 C— CR 3 c) 𝑅3 C— OH d) 𝑅3 C— O— C𝑅3
295. 𝐺𝑒𝑚 dihalides on treatment with alcoholic KOH give
a) Alkyne b) Alkene c) Alkane d) All of these
296. The presence of Ag ion increases the solubility of alkenes due to the formation of
+
a) b) c) d)
a) b) c) d)
327. On passing electric discharge through graphite in presence of H2 the compound formed is:
a) CH4 b) C2 H6 c) C2 H2 d) All of these
328. Propene reacts with Cl2 at 400-600C to give:
a) 1,2-dichloropropane b) Allyl chloride c) No reaction d) Polyvinyl chloride
329. Methane reacts with oxygen at 100 atm and 300C in presence of Cu to give:
a) Acetaldehyde b) Methyl alcohol c) Acetic acid d) Ethyl alcohol
330. Ethylene is used in making:
a) Anti-freeze b) Solvent c) Fumigant d) All of these
331. The main constituent of light oil fraction is:
a) Benzene b) Toluene c) Phenol d) Naphthalene
332. The major product in the acid catalysed dehydration of 2-pentanol is:
a) 4-pentene b) 3-pentene c) 2-pentene d) 1-pentene
333. Which gas is commonly used in welding?
a) C2 H4 b) C2 H2 c) CH4 d) C2 H6
334. The synthesis of 3-octyne is achieved by adding a bromoalkane into a mixture of sodium amide
and an alkyne. The bromoalkane and alkyne respectively are
a) BrCH2 CH2 CH2 CH2 CH3 and CH3 CH2 C ≡ CH b) BrCH2 CH2 CH3 and CH3 CH2 CH2 C ≡ CH
c) BrCH2 CH2 CH2 CH2 CH3 and CH3 C ≡ CH d) BrCH2 CH2 CH2 CH3 and CH3 CH2 C ≡ CH
335. Which is most acidic of the following?
a) Methane b) Acetylene c) 1-butene d) 𝑁𝑒𝑜-pentane
336. Addition of HI on double bond of propene yields isopropyl iodide and not 𝑛-propyl iodide as the major
product, because addition proceeds through:
a) A more stable carbonium ion
b) A more stable carbanion
c) A more stable free radical
d) None of the above
337. Correct statement about 1,3-dibutene
a) Conjugated double bonds are present b) Reacts with HBr
c) Forms polymer d) All of the above
338. Preparation of ethane by electrolysis of aqueous solution of potassium acetate is called
a) Wurtz reaction b) Kolbe’s synthesis
c) Grignard reaction d) Sabatier-Sendersen’s reaction
339. 𝐴(C H ) →H2 ,Ni O
𝐵(C H ) →
3 /H2 O/Zn
CH CHO
4 6 4 8 3
1 mole
Thus, 𝐴 and 𝐵 are
a) b)
The reaction of
with HBr gives predominantly
a) b)
c) d)
348. The product formed when acetylene is passed through red hot tube is:
a) Benzene b) Cyclohexane c) Neoprene d) Ethane
349. The product formed when toluene is heated in light with 𝐶𝑙2 and in absence of halogen carrier is
a) Chlorobenzene b) Gammexane c) Benzotrichloride d) DDT
350. Among the following statement on the nitration of aromatic compounds, the false one is
a) The rate of nitration of benzene is almost the same as that of hexadeuterobenzene
b) The rate of nitration of toluene is greater than that of benzene
c) The rate of nitration of benzene is greater than that of hexadeuterbenzene
d) Nitration is an electrophilic substitution reaction
351. Reaction of one molecule of HBr with one molecule of 1, 3-butadiene at 40℃ gives predominantly
a) 1-bromo-2-butene under kinetically controlled conditions
b) 3-bromobutene under thermodynamically controlled conditions
c) 1-bromo-2-butene under thermodynamically controlled conditions
d) 3-bromobutene under kinetically controlled conditions
352. Which of the following compound is aromatic?
a) b) c) d)
𝑋 is
𝑅 − C − Cl 𝑅−C−𝑅 𝑅−C−H
a) || b) || c) || d) 𝑅 − O − 𝑅
O O O
356. A mixture ofCS2 and H2 S on passing over heated Cu gives:
a) C2 H6 b) CH4 c) C3 H8 d) None of these
357. Photochemical chlorination of alkane is initiated by a process of:
a) Pyrolysis b) Substitution c) Homolysis d) Peroxidation
358. Under which one of the following conditions, does the reaction,
?
CH ≡ CH + CH3 OH → CH3 O − CH = CH2 take place?
a) NH4 OH⁄80℃ b) Conc. H2 SO4 ⁄160℃
c) Anhydrous ZnCl2 ⁄150℃ d) CH3 OK⁄160 − 200℃
359. Which one is correct for the given change?
b)
a)
b)
c)
d)
362. (1)NaNH2 H2
CH3 C ≡ CH → 𝐴 → 𝐵
(2) CH3 CH2 Br Lindlar′ s catalyst
What is 𝐵 in the above reaction?
a) b)
c) d)
363. The gas believed to be the cause of explosion in coal-mines or fire damp is:
a) Methane b) Ethane c) C3 H8 d) CO
364. Addition of HBr to propylene in presence of benzoyl peroxide, follows
a) Markownioff’s rule b) Baeyer’s rule
c) Carbanion mechanism d) 𝑎𝑛𝑡𝑖-Markownioff’s rule
365. 2-phenyl propene on acidic hydration gives,
a) 2-phenyl-2-propanol b) 2-phenyl-1-propanol
c) 3-phenyl-1-propanol d) 1-phenyl-2-propanol
366. CH2 = CH2 is also called a:
a) Monomer b) Polymer c) Isomer d) Equimer
367. Halogenation of alkanes is an example of:
a) Electrophilic substitution
b) Nucleophilic substitution
c) Free radical substitution
d) Oxidation
368. The most stable isomer of 1,2-dichloroethane is:
a) Staggered b) Gauche c) Eclipsed d) Partially eclipsed
369. Which does not decolourizeBr2 water?
a) b)
c) d)
375.
is called:
a) Wurtz’s reaction b) Kolbe’s reaction c) Sabatier and Senderens d) Carbylamines reaction
reaction
376.
a) b) c) d)
a) b) c) d)
396. Which products are formed during the addition of Br2 on ethylene in presence of aqueous NaNO3 solution?
a) CH2 Br. CH2 ONO2
b) CH2 Br. CH2 Br
c) CH2 (ONO2 ). CH2 ONO2
d) Both (a) and (b)
397. Alkanes containing…..carbon atoms are converted into an aromatic hydrocarbon, when heated in presence
of Cr2 O3 on Al2 O3
a) 6 to 10 b) 4 to 8 c) 3 to 6 d) 5 to 6
398. Chlorination of toluene in the presence of light and heat followed by treatment with aqueous
NaOH solution gives
a) 𝑜-cresol b) 𝑝-cresol
c) Benzoic acid d) 2,4-dihydroxytoluene
399. Toluene can be converted into benzaldehyde by oxidation with
a) KMnO4 /alkali b) CrO2 Cl2 c) K 2 Cr2 O7 /H2 SO4 d) O2 /V2 O5
400. HgSO 4
CH3 − CH2 − C ≡ CH → 𝐴
H2 SO4
The compound A is
O
a) || b) CH3 − CH2 − CH2 − CHO
CH3 − CH2 − C − CH3
c) CH3 − CH2 − CH2 − COOH d) None of the above
401. When acetylene is passed through dil. H2 SO4 in presence of HgSO4 , the compound formed is
a) Ether b) Acetaldehyde c) Acetic acid d) Ketone
402. The reagent used for dehydration is:
a) Conc. H2 SO4 b) P2 O5 c) Al2 O3 d) All of these
403. A hydrocarbon has the formula C3 H4 . To find out whether it contains two double bonds or triple bonds,
the following test is performed:
a) Passed through ammoniacalAgNO3
b) Treated with Baeyer’s reagent
c) Treated with Fehling’s solution
d) Treated with Br2 water
404. The chemicals and the reaction conditions required for the preparation of ethane are
a) C2 H5 I, Zn − Cu, C2 H5 OH b) CH3 Cl, Na, H2 O
c) KOOC − CH = CH − COOK, electrolysis d) CH3 CO2 Na, NaOH, CaO, ∆
405. Formation of alkane by the action of zinc on alkyl halide is called
a) Wurtz reaction b) Kolbe’s reaction c) Ulmann’s reaction d) Frankland reaction
406.
a) b) c) d)
415. Aniline is treated with a mixture of sodium nitrite and hypophosphorus acid, the product formed
is
a) Aniline diazonium hypophosphate b) Benzene
c) Anilinium hypophosphite d) Aniline diazonium hypophosphite
416. Hexachloroethane is also called
a) DDT b) TNT c) Artificial camphor d) BHC
417. In presence of nickel cyanide, acetylene gives
a) Benzene b) Cyclooctatetraene c) Cyclohexatriene d) Cyclobutadiene
418. Conjugated double bonds are present in:
a) Propylene b) Isobutylene c) Butylene d) 1,3-butadiene
419. Normal alkanes can undergo sulphonation if they contain:
a) 4 carbon atoms
b) 5 carbon atoms
c) At least 6 carbon atoms
d) 3 carbon atoms
420.
Br
a) CH3 Br − CH = CH2 b) |
CH3 − C = CH2
c) CH3 CH = CHBr d) None of the above
432. Observe the following reactions and predict the nature of A and B.
a) b)
c) d)
433. HBr is added to CH3 — CH = CH2 in presence of peroxides. The resultant compound is:
a) CH3 CHBrCH3 b) C2 H5 CH2 Br c) CH2 = CH2 CH2 Br d) None of these
434. Amount of Br2 required to react with 5 g pentene to form monobromo derivative is:
a) 11.11 g b) 11.43 g c) 5.55 g d) None of these
435. The compound (i) decolourisesKMnO4 (ii) forms ozonide with ozone and (iii) undergoes polymerization.
It will be:
a) C6 H6 b) C3 H8 c) C2 H4 d) C2 H6
436. The strongest 𝑜𝑟𝑡ℎ𝑜/𝑝𝑎𝑟𝑎 directing group is
a) −NH2 b) −CH3 c) −Cl d) −C2 H5
437. Which of the following species will be aromatic?
d) None of these
a) b) c)
438. When chlorine is passed through warm benzene in presence of the sunlight, the product obtained
is
a) Benzotrichloride b) Chlorobenzene c) Gammexane d) DDT
439. The C = C bond distance in an organic compound is1.34 Å. It can be
a) Butene b) Hexatriene c) Cyclohexatriene d) Any of these
440. The lowest possible alkane with ethyl group as substituents possesses mol. mass equal to:
a) 16 b) 72 c) 84 d) 128
441. The reagent(s) for the following conversion,
cis/are
a) Alcoholic KOH b) Alcoholic KOH followed by NaNH2
c) Aqueous KOH followed by NaNH2 d) Zn⁄CH3 OH
442. Aqueous H2 SO4 reacts with 2-methyl-1-butene to give predominantly:
a) Isopentyl hydrogen sulphate
b) 2-methyl-3-butene
c) 2-methyl-1-butene
d) Secondary butyl hydrogen sulphate
443. The number of conformation(s) for ethane is/are:
a) 1 b) 2 c) 3 d) Infinite
444. The test for unsaturation is confirmed by the decolourisation of which of the following?
a) Iodine water b) CuSO4 solution c) Bromine water d) All of these
445. Which does not react with chlorine in dark?
a) CH4 b) C2 H2 c) C2 H4 d) CH3 CHO
446. The ozonolysis of isobutene gives:
a) CH3 CHO b) CH3 COCH3 and HCHO c) CH3 CH2 OH d) CH3 OH
447. Which compound on reductive ozonolysis forms only glyoxal?
a) Ethyne b) Ethene c) Ethane d) 1,3-butadiene
448. The reaction,
a) b) c) d)
a) b) c) d)
a) Clemmensen reduction
b) Fisher-Spier reduction
c) Birch reduction
d) Arndt-Eistert reduction
473. Which one of the following compounds will react with methyl magnesium iodide?
a) CH3 CH2 CH2 CH2 CH3 b) CH3 CH = CH − CH = CH2
c) CH3 − C ≡ C − CH2 CH3 d) CH3 CH2 CH2 C ≡ CH
474. Degree of unsaturation in the following compound is
a) 1° b) 2° c) 3° d) 4°
475. Suitable reagents A and B for the following reactions are
a) b)
c)
The hydrocarbon is :
a) Cyclohexane b) Benzene c) Cyclohexene d) Cyclobutane
484. Alkyl halides react with dialkyl copper reagents to give
a) Alkenyl halides b) Alkanes
c) Alkyl copper halides d) Alkenes
485.
Thus, 𝐴 is
a) (CH3 )2 CHCH = CHCH = CH2 b) (CH3 )2 C = CH − CH = CH2
c) CH3 CH = CH − CH = CH − CH = CH2 d) none of the above
486. In the series,
NaNH2 CH3 I HgSo4
C2 H5 → 𝑋→ 𝑌→ 𝑍
H2 SO4 ,H2 O
The compound Z is
a) CH3 CH2 CH = CH2 b) CH3 COCH3 c) CH3 CHO d) CH3 CH2 CH2 CHO
487. Paraffin dissolves in:
a) Distilled water b) Benzene c) Methanol d) Salt water
488. Which cannot be prepared by Kolbe’s electrolytic reaction using single salt?
a) CH4 b) C2 H6 c) C4 H10 d) H2
489. Which will react withNaBH4 ?
a) Benzoic acid b) Benzamide c) Cyclohexanone d) Acetic acid
490. When methane is made to react with a halogen (𝑋2 ), halides are formed, the order of reactivity is:
a) F2 > 𝐶l2 > 𝐵r2 > I2 b) Cl2 > F2 > 𝐵r2 > I2 c) I2 > 𝐵r2 > 𝐶l2 > F2 d) Cl2 > F2 > I2 > 𝐵r2
491. Which of these does not follow 𝑎𝑛𝑡𝑖 −Markownikoff’s rule?
a) 2-butene b) 1-butene c) 2-pentene d) 2-hexene
492. Acetylene reacts with HCN in the presence of Ba(CN)2 to yield
a) 1,1-dicyanoethane b) 1,2-dicyanoethane c) Vinyl cyanide d) None of these
493. An alkyl bromide (X) reacts with Na to form 4, 5-diethyl octane. Compound (X) is:
a) CH3 (CH2 )3 Br
b) CH3 (CH2 )5 Br
c) CH3 (CH2 )3 CHBr. CH3
d) CH3 (CH2 )2 CHBrCH2 CH3
494. To avoid lead pollution, a new anti-knock compound is used. It is:
a)
a) b) c) d)
508. Propene, CH3 — CH = CH2 can be converted into 1-propanol by oxidation. Which set of reagents among the
following is ideal to effect the conversion?
a) Alkaline KMnO4 b) B2 H6 and alk. H2 O2 c) O3 /zinc dust d) OsO4 /CHCl3
509. Compound which gives acetone on ozonolysis
a) CH3 − CH = CH − CH3 b) (CH3 )2 C = C(CH3 )2
c) C6 H5 CH = CH2 d) CH3 CH = CH2
510. Toluene, when treated with Br2 /Fe, gives p-bromotoluene as the major product because the – CH3 group
a) Is 𝑚𝑒𝑡𝑎 directing b) deactivates the ring
c) activates the ring by hyperconjugation d) None of the above
511. Alkynes occur in nature in the:
a) Free state b) Partially free state c) Not in the free state d) None of the above
512. Which of the following will have least hindered rotation about carbon-carbon bond?
a) Ethane b) Ethylene c) Acetylene d) Hexachloroethane
513. Identify Z in the series,
HBr aq.KOH NaCO3
CH2 = CH2 → 𝑋→ 𝑌→ 𝑍
I2 excess
a) C2 H5 I b) C2 H5 OH c) CHI3 d) CH3 CHO
514. Action of NH3 over C2 H2 at high temperature gives:
a) Amine b) Furan c) Thiophene d) Pyrrole
515. Wurtz reaction converts alkyl halide into alkane when it is made to react with
a) Na in alcohol b) Na in dry ether c) Zn in alcohol d) Zn in dry ether
516. Polyethylene is a resin obtained by polymerization of:
a) Butadiene b) Ethylene c) Isoprene d) Styrene
517. Cyclohexane (C6 H12 ) a hydrocarbon, floats on water because:
a) It is immiscible with water
b) Its density is less than that of water
c) It is a non-polar substance
d) It is immiscible and lighter than water
518. Which of the following are produced from coaltar?
a) Synthetic dyes b) Drugs c) Perfumes d) All of these
519. The reduction of an alkyne to alkene using lithium metal in liquid ammonia as solvent results into
a) 𝑐𝑖𝑠 addition of hydrogen atoms
b) 𝑡𝑟𝑎𝑛𝑠 addition of hydrogen atoms
Both 𝑐𝑖𝑠 and 𝑡𝑟𝑎𝑛𝑠 additions of hydrogen atoms. The relative amounts of the two depends on
c)
temperature
d) Both 𝑐𝑖𝑠 and 𝑡𝑟𝑎𝑛𝑠 additions of hydrogen atoms. The relative amounts depend on the nature of alkyne
520. Propene on reaction with hypochlorous acid to give
a) b)
c) d)
521. A mixture of nitrogen and acetylene, on passing electric spark through it gives:
a) Hydrogen and carbon b) Hydrogen cyanide c) Nitromethane d) Nitroethane
522. In the sequence of reactions,
HBr AgCN ( H)
C2 H4 → 𝑋→ 𝑌 → 𝑍,
H2 /Ni
Compound Z is
a) N-methyl ethanamine b) N-propylamine
c) N, N-dimethylamine d) Ethyl cyanide
523. Which one of these is not true for benzene?
a) It forms only one type of monosubstituted product.
b) There are three carbon-carbon single bonds and three carbon-carbon double bonds
c) The heat of hydrogenation of benzene is less than the theoretical value.
d) The bond angle between the carbon-carbon bonds is 120°.
524. Presence of a nitro group in a benzene ring
a) Activates the ring towards electrophilic substitution
b) Renders the ring basic
c) Deactivates the ring towards nucleophilic substitution
d) Deactivates the ring towards electrophilic substitution
525. The major product in the reaction of 2-butyne with Li/liq. NH3 is
a) b)
534.
Alkene
a) b) c) d)
535. A solution of sodium salt of fatty acid was electrolysed during Kolbe’s reaction. The solution left after
electrolysis is:
a) Richer in NaOH b) Richer in H2 SO4 c) Richer in sodium salt d) All of these
536. Sample of 2,3-dibromo-3-methylpentane is heated with zinc dust. The resulting product is isolated and
heated with HI in the presence of phosphorus. Indicate which is the structure that represents the final
organic product in the reaction?
a)
b)
c)
d)
537. Which compound does not give precipitate with ammoniacal silver nitrate solution?
a) C2 H5 − C ≡ CH b) CH3 − C ≡ C − CH3
CH3
c) | d) Ph − CH2 − C ≡ CH
CH3 − CH − C ≡ CH
538. Hydroxylation of propyne in the presence of HgSO4 /H2 SO4 is initiated by the attack of:
a) Carbene b) Free radical c) Electrophile d) Nucleophile
539. Benzene vapour mixed with air when passed over V2 O5 catalyst at 775 K gives
a) Glyoxal b) Oxalic acid c) Maleic anhydride d) Fumaric acid
540. Kolbe’s synthesis on electrolysis of sodium salt of butanoic acid gives:
a) 𝑛-hexane b) Isobutene c) Butane d) Ethene
541. Which among the following is aromatic?
a) b) c) d)
542. The neutral wax called Ozokerite found near petroleum well is a mixture of:
a) Solid halides b) Solid hydrocarbons c) Solid alcohols d) None of these
543.
Identify A:
d) None of these
a) b) c)
a) b) c) d)
a)
b)
c)
d)
a) SeO2 b) O3 , Zn⁄H2 O
c) O3 , H2 O2 − CH3 COOH d) PCC
555. The chemical reactivity of ethylene is due to:
a) Short carbon to carbon bond distance
b) High double bond energy
c) Trigonal planar structure
d) Presence of 𝜋-electrons
556. Which of the following species could be expected to exhibit aromatic character?
b)
a) b)
c) d)
a) b) c) d)
573. Pure acetylene has sweet ethereal smell while impure smells like garlic due to presence of:
a) NH3 b) PH3 c) AsH3 d) H2 S
574. An alkyl halide by formation of its Grignard reagent and heating with water yields propane. What
is the original alkyl halide?
a) Methyl iodide b) Ethyl iodide c) Ethyl bromide d) Propyl bromide
575. 1-propyne on treatment with dilute H2 SO4 in presence of HgSO4 gives acetone. The change is due to:
a) Hyperconjugation b) Resonance c) Tautomerism d) None of these
576. O2 required for complete oxidation of 1 litre of ethane at NTP is:
a) 3.5 litre b) 0.156 mole c) 5.00 g d) All of these
577. In the following sequence the product 𝐷 is,
HBr HBr KOH ale. NaNH2
CH ≡ CH → 𝐴 → 𝐵 → 𝐶→ 𝐷:
a) Ethanol b) Ethane c) Ethyne d) Ethanal
578. Which of the following compounds react with HBr obeying Markownikoff’s rule?
a) CH2 = CH2 b)
c) d)
1. 2.
3. 4.
a) 1 and 4 b) 2 and 3 c) 1 and 2 d) 1 and 3
582. A mixture of ethane, ethene and ethyne is passed through ammoniacalAgNO3 solution. The gases which
remain unreacted are:
a) Ethane and ethene b) Ethane and ethyne c) Ethene and ethyne d) Ethane only
583. In the reaction,
Oxidation NaOH Soda lime
C6 H5 CH3 → 𝐴→ 𝐵→ 𝐶
The product 𝐶 is
a) C6 H5 OH b) C6 H6 c) C6 H5 COONa d) C6 H5 ONa
584. (I) BH3 .THF HgSO4
𝐴← CH3 C ≡ CH → 𝐵
(II)H2 O2 ,OH− H2 SO4
Identify 𝐴 and 𝐵
a) CH3 CHO, CH3 COCH3 b) CH3 CH2 CHO, CH3 COCH3
c) CH3 CH2 CHO, CH3 COCH2 CH3 d) HCHO, CH3 COCH3
585. Cyclobutadiene is said to be
a) aromatic b) aliphatic c) non-aromatic d) None of these
586. Acetylene reacts with hypochlorous acid to form
a) Cl2 CHCHO b) ClCH2 COOH c) Cl3 COCl d) ClCH2 CHO
587. To enable easy detection of gas leakage from cylinders, the substance added to L.P.G. is:
a) Glycols b) Phenols c) Thioalcohols d) Glycerols
588. Octane no. of 2,3,3-trimethylbutane has been assumed to be:
a) 100 b) −45 c) 124 d) Zero
589. 𝐶4 𝐻6 may contain
a) One double bond b) Two double bond c) One triple bond d) Both (b) and (c)
590. Which of the following compounds can form metallic derivatives?
a) Ethane b) Propyne c) 2-butyne d) 2-butene
591. Increasing order of volatility of C2 H6 , C2 H4 , C2 H2 and C6 H6 is:
a) C6 H6 , C2 H6 , C2 H4 , C2 H2 b) C2 H2 , C2 H4 , C2 H6 , C6 H6 c) C6 H6 , C2 H2 , C2 H4 , C2 H6 d) C2 H2 , C2 H6 , C2 H4 , C6 H6
592. Octane no. of a fuel can be increased by:
a) Isomerism b) Alkylation c) Reforming d) All of these
593. 1-propanol on dehydration with H2 SO4 produces:
a) CH3 − CH = CH2
b) CH3 − CH = CH − CH3
c) CH3 CH2 CH2 OCH2 CH2 CH3
d) CH3 CH2 CH2 CH2 CH = CH2
594. Propadiene, C3 H4 molecule contains:
a) Two 𝑠𝑝2 and one 𝑠𝑝-hybrid carbon
b) One 𝑠𝑝2 and two 𝑠𝑝-hybrid carbons
c) One 𝑠𝑝2 and three 𝑠𝑝-hybrid carbons
d) None of the above
595. Catalyst used in dimerization of acetylene to prepare chloroprene is:
a) HgSO4 + H2 SO4 b) Cu2 Cl2 c) Cu2 Cl2 + NH4 Cl d) Cu2 Cl2 + NH4 OH
596. Cyclopentene on treatment with alkaline KMnO4 gives:
a) Cyclopentanol
b) 𝑡𝑟𝑎𝑛𝑠-1,2-cyclopentanediol
c) 𝑐𝑖𝑠-1,2-cyclopentanediol
d) 1 : 1 mixture of 𝑐𝑖𝑠-and 𝑡𝑟𝑎𝑛𝑠-1,2-cyclopentanediol
597. 3Cl2 ,Heat Fe⁄Br2 Zn⁄HCl
C7 H8 → 𝐴→ 𝐵→ 𝐶
Here, the compound 𝐶 is
a) 3-bromo 2,4,5,6-trichlorotoluene b) 𝑜-bromo toluene
c) 𝑝-bromo toluene d) 𝑚-bromo toluene
598. Naphalene is an example of
a) Polynuclear hydrocarbon b) alicyclic compound
c) heterocyclic compound d) aliphatic compound
599. Which of the following will give 𝑡𝑟𝑎𝑛𝑠-diols?
a) b)
c) d)
a) b) c) d)
b)
c)
a) I > 𝐼𝐼 > 𝐼𝐼𝐼 > 𝐼𝑉 b) IV > 𝐼𝐼𝐼 > 𝐼𝐼 > 𝐼 c) I > 𝐼𝐼𝐼 > 𝐼𝑉 > 𝐼𝐼 d) II > 𝐼𝐼𝐼 > 𝐼 > 𝐼𝑉
646. The product B is:
HI
CH3 . CH2 . C = CH + HCI ⟶ B → C
a) b) c) d)
a) C6 H5 CHCl2 b) c)
654. An alkene, obtained by the dehydration of an alcohol (A), on ozonolysis gives two molecules of
acetaldehyde for every molecule of alkene. The alcohol (A) is:
a) b) c) d)
661. Lindlar′ s Na in
[ 𝐴] ← CH3 − C ≡ C − CH3 → [𝐵]
catalyst liq.NH3
[A] and [B] are respectively
a) 𝑐𝑖𝑠, 𝑡𝑟𝑎𝑛𝑠-2-butene b) Both 𝑡𝑟𝑎𝑛𝑠-2-butene
c) 𝑡𝑟𝑎𝑛𝑠, 𝑐𝑖𝑠-2-butene d) Both 𝑐𝑖𝑠-2-butene
662. Which of the following reacts with KMnO4 but does not react withAgNO3 ?
a) C2 H6 b) CH4 c) C2 H4 d) C2 H2
663. Octane number 116 is given for:
a) 2,2,2-trimethyl pentane
b) 2,3,4-trimethyl pentane
c) 2,2,3-trimethyl butane
d) 2,2,4-trimethyl butane
664. Which of the following statements is incorrect?
a) Acetylene is explosive above 2 atm
b) It is transported by dissolving in acetone
c) It has unpleasant garlic odour
d) It is used in the manufacture of Lewisite
665. Formation of ethylene from ethyl bromide is a case of:
a) Addition reaction
b) Substitution reaction
c) Elimination reaction
d) Rearrangement reaction
666. The most stable alkene is,
a) 𝑅2 𝐶 = 𝐶𝑅2 b) 𝑅CH = CH𝑅 c) CH2 = CH2 d) 𝑅CH = C𝑅2
667. Ethylene can be prepared by electrolysis of an aqueous solution of:
a) Sodium acetate b) Sodium succinate c) Sodium fumarate d) Sodium propionate
668. HBr reacts with CH2 = CH − OCH3 under anhydrous conditions at room temperature to give
a) CH3 CHO and CH3 Br b) BrCH2 CHO and CH3 OH
c) BrCH2 − CH2 − OCH3 d) H3 C − CHBr − OCH3
669. Identify 𝑍 in the following series?
HBr Hydrolysis Na2 CO3
CH2 = CH2 → 𝑋→ 𝑌→ 𝑍
I2 excess
a) C2 H5 I b) CHI3 c) CH3 CHO d) C2 H5 OH
670. Reactive species in halogenation of benzene in cold and dark
a) Cl• b) Cl+ c) Cl− d) None of these
671. An organic alkadiene on reductive ozonolysis produces
(i)acetaldehyde
(ii)acetone
(iii)2-methylpropane-1, 3-dial
The formula of alkadiene will be
CH3 C = CHCHCH = CHCH3 CH3 CHCH = CCH = CHCH3
a) | | b) | |
CH3 CH3 CH3 CH3
CH3 C = CHCHC = CHCH3 CH3 CH2 CHCH = CHC = CH2
c) | | d) | |
CH3 CH3 CH3 CH3
672. Synthetic petrol and kerosene can be obtained by passing……under heat and pressure over coal.
a) O2 b) H2 c) N2 d) CO2
673. A hydrocarbon containing 2 carbon atoms give Sabatier and Senderen’s reaction but does not give
precipitate with ammoniacal silver nitrate solution. The hydrocarbon in question is:
a) Ethane b) Acetylene c) Ethylene d) None of these
674. Acetylene can be converted to higher alkyne using the following sequence of reactions:
a) Na, 𝑅𝑋 b) 𝑅Mg 𝑋, 𝑅 𝑋 c) Either of these two d) None of these
675. At low temperature, the slow addition of molecular bromine to H2 C = CH— CH2 — C ≡ CH gives:
a) CH2 = CH— CH2 — CBr = CHBr
b) BrCH2 — CHBr— CH2 — C ≡ CH
c) H2 C = CH— CH2 — CH2 — CBr3
d) CH3 — CBr2 — CH2 — C ≡ CH
676. Which of the following statement is correct?
a) Benzene has a tetrahedral geometry like an alkane
b) Benzene is aromatic while naphthalene is not
c) Benzene and Cyclohexane are both aromatic
d) Benzene behaves more like and alkane than an alkene
677. CaC + H O → 𝐴 H →
2 SO4 /HgSO4
𝐵
2 2
Identify 𝐴 and 𝐵 in the given reaction
a) C2 H2 and CH3 CHO b) CH4 and HCOOH
c) C2 H4 and CH3 COOH d) C2 H2 and CH3 COOH
678. The correct boiling point order for corresponding hydrocarbons is:
a) Alkyne>alkane>alkene
b) Alkane>alkene>alkyne
c) Alkyne>alkene>alkane
d) Alkene>alkyne>alkane
679.
Identify A and B
a) b)
c) d)
680. Electrolysis of cold concentrated aqueous solution of potassium methyl succinate yields:
a) Ethane b) Ethyne c) Propene d) Ethane-1,2-diol
681. An alkene gives two moles of HCHO, one mole of CO2 and one mole of CH3 COCHO on ozonolysis.
What is its structure?
CH3
a) CH2 = C = CH − CH2 − CH3 b) |
CH2 = CH − CH − CH = CH2
CH2 = C = C − CH3 CH3
c) | d) |
CH3 CH2 = C = C − CH = CH2
682. Alkyl halides get converted to alkenes through:
a) Electrophilic b) Nucleophilic addition c) Elimination reaction d) Hydrolysis
substitution
683. In the complete combustion of C𝑛 H2𝑛+2 , the number of oxygen moles required is:
𝑛 𝑛+1 3𝑛 + 1 𝑛+2
a) ( ) O2 b) ( ) O2 c) ( ) O2 d) ( ) O2
2 2 2 2
684. When CH3 CH2 CHCI2 is treated with NaNH2 the product formed is:
a)
b)
10 (c)
C3 H8 + 5O2 → 3CO2 + 4H2 O
11 (a)
2 (c) Follow cleavage of two bonds at multiple bonding
Bees wax is myricyl palmitate, 𝑖. 𝑒., position during ozonolysis.
C15 H31 COOC30 H61 . 12 (a)
3 (a) AlCl
CH2 = CH2 + CH3 COCl → CH3 COCH2 CH2 Cl.
The knocking order is:
13 (b)
Straight > branched >olefins>arenes.
chain alkane chain alkane It is a Corey House synthesis of alkanes.
4 (d) 14 (b)
Follow peroxide effect. C2 H2 is used for artificial ripening of fruits.
5 (b) C2 H4 for natural ripening.
Successive homologous differ by —CH2gp. 15 (a)
6 (c) Follow Markownikoff’s rule for addition.
1, 2-dihalogen (𝑣𝑖𝑐𝑖𝑛𝑎𝑙) derivatives of the 16 (b)
alkanes on reaction with zinc dust and Ethane gives a mixture of nitroethane and
methanol produces alkenes by loss of two nitromethane.
halogen atoms (dehalogenation). CH3 − CH3 + HNO3
Alcohol⁄∆ Ethane
CH3 − CH − CH2 + Zn → CH3 CH = CH2 673 K
→ CH3 − CH2 − NO2 + CH3 NO2
| | propylene −H2 O
Propane
Lindlar’s catalyst prevents further reduction of The reaction is used to yield aromatic
ethane to ethane. hydrocarbons.
69 (c) 81 (d)
Am. Cu2 Cl2 gives red ppt.with alkyne. Alkanes are non-polar and have almost non-polar
70 (d) bonds C—H and non-polar bond C—C. They show
∆
(C2 H5 )4 NOH → (C2 H5 )3 N + C2 H4 + H2 O only substitution reactions in presence of light.
72 (d) 82 (d)
Ozonolysis involves the breaking of double
bond and insertion of O atoms in place of
double bond. Therefore, the structure of
alkene is as To identify alkene (from ozonolysis
products)place these products with O-atoms
face to face. Replace O-atoms by = (double
bond).
74 (b)
Alkenes on treatment with diazomethane
(CH2 N2 ) in the presence of UV light give
cyclopropane and its derivatives. This addition
takes place across the double bond
83 (c)
By the reaction of benzene with ethylene in
presence of anhydrous AlCl3 , ethylbenzene is
75 (c)
produced.
Fluorination is highly explosive and occurs
violently.
76 (b)
CH3 CH2 CH2 CH2 CH2 Cl; CH3 CH2 CH2 CHClCH3;
CH3 CH2 CHClCH2 CH3
77 (d) 84 (b)
Double bond is broken to give ketone and acid.
85 (a)
Toluene has electron releasing group (CH3 ) thus
it most reactive towards electrophilic nitration
86 (c)
𝐶𝑛 𝐻2𝑛 𝑂 = 44
𝐶𝑛 𝐻2𝑛 = 44 − 16 = 28 95 (c)
∴𝑛=2 Reactivity towards electrophilic substitution
So, CH3 − CH = CH − CH3 is increases as the electron density in the benzene
symmertricalalkene. ring increases. Since 𝐶𝐻3 is a strong electron
Thus, donating group thus can be most readily
I.O3 sulphonated
CH3 − CH = CH − CH3 → 2CH3 − CH = O 96 (b)
II.Zn/H O 2
2-butene acetaldehyde OH
87 (b) |
H2 SO4
Conversion of propene to propanol is CH2 = CH − CH3 + H2 O → CH2 − CH
hydration. − CH3
OH Propylene isopropyl
| alcohol
H2 SO4
CH3 − CH = CH2 + H2 O → CH3 − CH Thus, in this reaction isopropyl alcohol is
− CH3 formed.
Propene propanol-2 98 (c)
88 (c) CaC2 + 2H2 O ⟶ Ca(OH)2 + C2 H2
The process is called aromatization. C2 H2 + Cu2 Cl2 ⟶ CuC ≡ CCu
89 (c) (Red ppt.)
CH4 + 2O2 ⟶ CO2 + 2H2 O 100 (a)
20 50 0 0 According to Huckel’s rule, an aromatic
0 10 20 Liquid
90 (c) compound should have (4𝑛 + 2)𝜋-electrons.
Where, 𝑛 is an integer, 𝑖. 𝑒., 0, 1, 3, 4, … and
possesses unusual stability due to the
delocalisation of 𝜋-electrons.
102 (d)
give only one monosubstituted product.
The octane no. for 𝑛-heptane is zero.
Is symmetrical alkane and will give only one
103 (c)
monosubstituted product.
This is hydrogenation of alkane.
Also C𝑛 H2𝑛+2 , 𝑖. 𝑒. , 12𝑛 + 2𝑛 + 2 = 72
104 (a)
𝑛=5
Tar, 𝑖. 𝑒., pitch contains alkanes from C30 to C40
91 (b)
chain.
The number of disubstituted products of benzene
105 (a)
is three
Thermal decomposition of alkanes in the
absence of air is called cracking or
pyrolysis𝑒. 𝑔.,
1000℃
CH4 → C + 2H2
106 (c)
92 (b) The following are the necessary conditions
𝑅′ Mg𝑋 + HC ≡ C𝑅 → 𝑅′ H + 𝑅C ≡ CMg𝑋 for compound to be aromatic.
93 (a)
1. Molecule must be planar and cyclic.
Electrolysis
2CH3 COONa → 2CH3 COO− + 2Na+
At anode 2. Conjugated double bond must be
present.
107 (d)
115 (b)
CH2 = CH— CH = CH2 ; 𝑠𝑝2 − 𝑠𝑝 2 (C — C)bond B2H6
length is 1.34Å 6𝑅— CH = CH2 → 2(𝑅CH2 CH2 )3 B2
6H2 O2
1 2 3 4 2(𝑅CH2 CH2 )3 B2 → 𝑅CH2 CH2 OH + 2H3 BO3
108 (c) This process always gives alkanol-1 from alkane-
CH2 = CH − CH2 Cl + CH3 MgI → 1.
117 (b)
allyl chloride
Side chain hydrogen atoms are substituted in
presence of light or heat. Ring hydrogens are
substituted in presence of Lewis acid.
109 (c)
(i)Among alkanes boiling point increases with
increase in molecular mass.
(ii)Among isomeric alkanes the boiling point
decreases with branching due to decrease in
surface area.
𝑛-octane will have highest boiling point
because it has highest number of carbon
atoms and does not show branching.
118 (b)
110 (c)
Direct iodination of alkane is not possible because
of reversible nature of HI. It is therefore carried
out in presence of HgOor HIO3.
(addition reaction). CH4 + I2 ⟶ CH3 I + HI
111 (d) HgO + 2HI → HgI2 + H2 O
119 (b)
is aromatic.
It contains 3 double bonds (6𝜋 electrons).
According to Huckel rule (4𝑛 + 2)𝜋 = 6𝜋
electrons where, 𝑛 = 1
120 (b)
Since, the alkene of oxidation gives only acetic
acid, therefore, the alkene must be
To symmetrical containing two carbon-atoms on
determine alkene, place these products with either side of the double bond, 𝑖𝑒., 2-butene.
O-atoms face to face and replace O-atoms by KMnO4
=bond. CH3 CH = CHCH3 → 2CH3 COOH
114 (a) 122 (d)
The presence of dilH2 SO4 and mercury salts, When carbon is bonded to four other atoms,
alkynes add a molecule of H2 O to form aldehydes the angle between any pair of bonds =
or ketones 109°, 28′ (tetrahedral angle) but the ring of
cyclobutane is square with four angles of 90°.
So, deviation of the bond angle (angle strain)
in cyclobutane
= 109°28′ − 90°⁄2
= 19°28′⁄2
= 9°44′
123 (c)
Excess of Cl2 finally converts all products to CCl4 .
124 (a)
𝑛-heptane gives toluene; 𝑛-octane gives ethyl
benzene.
125 (a)
The H-atoms of terminal alkyne (𝑖𝑒. , H3 C −
C ≡ CH) is weakly acidic.
Liq.NH3
CH3 ≡ CH + NaNH3 → H3 C − CH
≡ CNa + NH3
126 (c)
NaOH
HCOONa → H2 + Na2 CO3
134 (b)
127 (c)
At 60° (low temperature) mononitration
Alkyl halides undergo reduction with red
phosphorus and hydrogen iodine occurs and nitrobenzene is obtained but at
Red P/HI 100℃, nitrobenzene further undergoes
CH3 CH2 CH2 I → CH3 CH2 CH3
150℃ electrophilic substitution and gives 𝑚-
128 (a) dinitrobenzene (as – NO2 is a 𝑚𝑒𝑡𝑎 −
CH4 diffuses rapidly because of low mol. wt. directing group).
129 (a)
1
Boiling point ∝ molecualr mass ∝ branching
145 (d)
These are characteristics of ozonolysis.
146 (a)
When a conjugated diene (diene) is heated with
an unsaturated compound (dienophile) in a
150 (a)
HBr
The first addition will occur on double bond. Thus, CH ≡ CH— CH2 — CH = CH2 → CH ≡
C— CH2 — CHBr— CH3 but in CH ≡ C— CH = CH2 , the addition will occur at CH ≡ C because the product
formed is conjugated alkadiene, which is more stable.
151 (b)
It is alicyclic or aliphatic unsaturated.
152 (a)
(C2 H5 )4 Pb on addition to gasoline increases its
octane no. by about 5 units.
153 (b)
On heating with
156 (d)
sodamide(NaNH2 in liq. NH3 ),alkynide is formed
CH3 CH2 CH − CH3
|
OH
H+ −H2O
→ CH3 − CH2 − CH − CH3 →
154 (c) |
+
Only alcoholic KOH gives H−O −H
dehydrohalogenation reaction. Ethyl chloride (Major)CH3 CH = CHCH3
reacts with alcoholic KOH as (Minor)CH3 CH2 CH = CH2
157 (d)
It is fact. Follow octane number. precipitate with 1-alkynes (terminal alkynes).
158 (a) CH3 − C ≡ CH + 2[Cu(NH3 )2 ]Cl →
KMnO4
CH3 C = CH3 → CH3 COCH3 + CH3 COOH CH3 − C ≡ C − Cu + 2NH4 Cl + 2NH3
∆
| (red ppt.)
CH3 165 (c)
159 (a) C—C bond involves 2𝑠𝑝3 − 2𝑠𝑝3 (𝜎) whereas, C—
1-Butyne reacts with NaNH2 to give sodium salt H bond involves 2𝑠𝑝3 − 1𝑠(𝜎) in alkanes.
while 2-butyne does not react. Only terminal 166 (c)
Ni/Al2 O3
alkynes are acidic. CH4 + H2 O → CO + 3H2
NaNH2
CH3 — CH2 — C ≡ C— H → No reaction 167 (c)
NH3 + CH3 — CH2 — C ≡ C Na
Terminal alkyne reacts with ammoniacalAgNO3
160 (c) solution give a whilteppt, therefore 𝑥 must be a
When an alkyl halide reacts with sodium in terminal alkyne. Thus, 𝑥 must be(CH3 )2 CHC ≡ CH
KMnO4
presence of dry ether, an alkane with the (CH3 )2 CHC ≡ CH → (CH3 )2 CHCOOH
double number of carbon atoms than the + [HCOOH]
parent halide, is obtained and this reaction is 168 (c)
Zn
known as Wurtz reaction. 𝑅CH = C𝑅1 𝑅2 + O3 → 𝑅CHO + 𝑅1 CO𝑅2
H2 O
4 3 2 170 (a)
CH3 − CH − CH − Cl Zn
CH2 Br— CH2 Br → CH2 = CH2 + ZnBr2
| |
171 (d)
CH3 CH3
An alkyne combine with a conjugated diene to
2-chloro-3-methyl butane
give an unconjugatedcycloalkadiene. This
3 2
Na
reaction is known as Diels-Alder reaction.
+CH3 − CH − CH − Cl →
Dry ether
−2NaCl
| |
CH3 CH3
6 5 4 3 2 1 172 (a)
CH3 − CH − CH − CH − CH − CH3 Now-a-days used in refineries.
| | | | 173 (b)
CH3 CH3 CH3 CH3 Kerosene contains alkanes from C12 to C16 .
2,3,4,5-tetramethyl hexane 174 (d)
161 (b) On treatment with alcoholic KOH, 1-
Na⁄Liq.NH3 chlorobutane gives 1-butene while 2-
CH3 CH2 C ≡ CH → CH3 CH2 C ≡ CNa+
∆ chlorobutane gives 2-butene (major) +1-
Considering the options given it appears butene (minor). Therefore, a mixture of 1-
correct. Na⁄liq. NH3 is known for metal butene +2-butene is formed.
dissolved reduction. Actually it is truth that 176 (a)
Na⁄liq. NH3 reduces internal triple bond and O
terminal double bond and do not reduce the ∥
terminal alkyne due to such alkylide (i)O3
𝑋 → C2 H4 O + CH3 CH2 − C − CH3
formation. (ii)Zn/AcOH
200 (d)
CH2 = CH − CH2 CH3
Butene-1
Pd/H2
→ CH3 − CH2 − CH2 − CH3
∆,pressure
butane
Other reagents are successful with polar
double bonds.
203 (a) 214 (b)
Hg2+ ⁄H+ Indane is commercial name of L.P.G.
Ph − C ≡ C − CH3 → Ph − C = CH − CH3
215 (a)
| Terminal alkynes react with
OH
ammoniacalAgNO3 to give silver salt as they
Ph − C = CH2 CH3
have acidic hydrogen.
||
CH3 − C ≡ CH + AgNO3 + NH4 OH →
O
CH3 − C ≡ C. Ag + NH4 NO3 + H2 O
(𝐴) 217 (a)
204 (b) Cyclo propane is the most unstable cyclic
Follow mechanism of Wurtz reaction.
compound. So, with bromine it gives an open
205 (c)
chain compound 1, 3-dibromopropane.
It is a non-terminal alkyne.
207 (b)
1, 2-bromo cyclopentane on heating with 1− in
acetone gives cyclopentene.
208 (b)
Terminal alkynes react with am. AgNO3 or 218 (c)
Addition of HBr to an alkene in the presence of
peroxide is the example of free radical addition
reaction
228 (b)
CH ≡ CH + HBr → CH2 = CHBr
219 (a) 229 (a)
Electrolysis
All H-atoms in 𝑛𝑒𝑜-pentane are equivalent thus, it CH3 CH2 COONa → CH3 (CH2 )4 CH3 + NaOH
will yield monochloro product + H2
220 (b) 230 (b)
Acetylenichydrogens are acidic because sigma 2CHCl3 + 6Ag ⟶ C2 H2 + 6AgCl
electron density of C − H bond in acetylene is 231 (d)
nearer to carbon, which has 50% 𝑠-character In the presence of ferric chloride, electrophilic
221 (c) substitution at 𝑜𝑟𝑡ℎ𝑜 and 𝑝𝑎𝑟𝑎 position take place
Follow text. 232 (b)
222 (c) Butyne reacts with Na⁄liq. NH3 to give 𝑡𝑟𝑎𝑛𝑠-
Wurtz reaction Alkyl halide reacts with product.
sodium in presence of dry ether forms alkane
is known as Wurtz reaction.
CH3 Br + 2Na + BrCH3
Ether 233 (c)
→ CH3 − CH3 + 2NaBr
CH3
223 (b)
|
It is an experimental fact. +NaNH2
224 (c) CH3 − CH2 − CH − C ≡ CH →
+O3
(i)Unsaturated hydrocarbons are more 3-methyl-1-pentyne
reactive than saturated hydrocarbons.
(ii)Among alkene and alkyne, alkene are
more reactive because C ≡ C is quite strong
bond.
∴ Correct order of reactivity CH3
Alkene>alkyne>alkane |
or C2 H4 > C2 H2 > C2 H6 CH3 − CH − CH − COOH + HCOOH
etheneethyne ethane Optically active carboxylic acid.
225 (b)
236 (a)
Bacteria
(C6 H10 O5 )𝑛 + 𝑛H2 O → 3𝑛CH4 + 3𝑛CO2 The mechanism of Wurtz reaction is:
226 (c) C2 H5 Br + Na ⟶ Ċ2 H5 + NaBr
It is a common method to prepare alkanes. Ċ2 H5 + Ċ2 H5 ⟶ C4 H10
Methane cannot be prepared by Wurtz The disproportionation of free radical gives
reaction. Ċ 2 H 5 + Ċ2 H 5 ⟶ C2 H 4
CH3 Br + 2Na + BrCH3 → C2 H6 + 2NaBr 237 (b)
ethane When sodium propionate is heated with
227 (b) sodalime, ethane is formed.
CaO
Symmetrical optical isomers are called CH3 CH2 COONa + NaOH → C2 H6 + Na2 CO3
mesomers. ethane
238 (c) reaction with alkyle halide. This is called
Dry ether
2CH3 − CHBr + 2Na → CH3 − CH − CH Friedel-Craft’s alkylation.
− CH3
| | |
CH3 CH3 CH3
Isopropyl 2,3-dimethyl
butane
bromide
239 (d) 250 (a)
AsCl3 on CH ≡ CH
molybdenum oxide (MoO), it gives methanal
(formaldehyde).
[MoO]
CH4 + 2[O] → HCHO + H2 O
formaldehyde
304 (d)
Propyne reacts with AgNO3 in NH3 to give
benzaldehyde while ppt. of silver acetylide and propene
294 (c) does not react with it. (Only terminal alkynes
Alkaline KMnO4 converts an H-atom to —OH gp.
react withAgNO3 in NH3 ).
295 (a)
CH3 − C ≡ CH + AgNO3 + NH3
𝐺𝑒𝑚dihalides on treatment with alcoholic KOH
give alkyne.
Propyne
→ CH3 − C ≡ C Ag
silver acetylide
(white ppt.)
296 (c)
CH3 − CH = CH2 + AgNO3 + NH3
Ag + ion increases the solubility of alkenes due
→ no reaction
to the formation of 𝑝𝜋 − 𝑑𝜋 bonding. 305 (a)
297 (c) Rotation of groups or atoms round single bond
CH ≡ CH + 2HCHO → HOH2 C − C produces conformation.
≡ C − CH2 OH 306 (a)
Acetylene 2, butyne-1, 4-diol A compound is said to have aromatic
298 (b) character if ring system is planar (with 𝑝-
NaOH+CaO
(CH3 )2 CHCOONa → (CH3 )2 CH2 + Na2 CO3 orbital) and there is complete delocalisation
299 (a) of 𝜋-electrons (lone pair may be taken for
Alkenes show electrophilic addition. delocalisation as relay electrons). This is true
301 (c) is conjugated cyclic system.
Methane cannot be produced by Wurtz
reaction, Kolbe’s electrolytic method and
reduction with H2 because, it has one carbon
atom. Huckel rule is followed by when electrons
Pure methane can be produced by the used in delocalisation=(4𝜋 + 2)
decarboxylation of sodium acetate. (including lone-pair)
CaO
CH3 COONa + NaOH → CH4 + Na2 CO3 Where, 𝑛=0, 1, 2, 3,….
Soda lime methane
302 (a)
4. ring is planar
367 (c)
Halogenation of alkanes is free radical
The X is substitution.
O 368 (a)
∥ Staggered form is more stable.
R − C − Cl 369 (b)
Alkene having all its H attached on double bond increases regularly with increasing number of
does not decolouriseBr2 water due to low carbon atoms
reactivity. 382 (b)
370 (d) (C2 H5 )4 is anti-knock agent and increase octane
R of RMgX reacts with acidic H to give alkane. no. of gasoline.
371 (a) 384 (b)
The carbon-carbon bond length in benzene It is a fact.
(1.39 Å) in between that of C − 385 (d)
It is definition.
C(1.54 Å)and C = C(1.34 Å)𝑖. 𝑒., in between
387 (a)
that of C2 H6 and C2 H4 .
When acetylene is passed through red hot
373 (c)
iron tube, benzene is formed as
Follow strainless ring theory.
Red hot tube
374 (c) 3C2 H2 → C6 H6
(𝑋)
Reaction (a) also gives C6 H6 (or 𝑋) as
Distillation
C6 H5 OH + Zn → C6 H6 + ZnO
389 (a)
CH3
|
(∵ In the product, −Br is𝑝𝑎𝑟𝑎to − CH3 − CH − C − CH3
CH3 and𝑚𝑒𝑡𝑎to − COOH. ) | |
375 (c) OH CH3
Hydrogenation of alkene or alkyne in presence of
3,3-dimethyl butane-2-ol
Ni is called Sabatier and Senderen’s reaction.
CH3 CH3
376 (b)
| |
Conc.H2 SO4
→ H3 C − C = C − CH3
−H2 O
2,3-dimethyl-2-butene
This reaction is an example of Friedel-Craft’s (major product)
reaction. 390 (a)
Mechanism: Fractional distillation of petroleum gives a large
number of products aliphatic and aromatic.
391 (a)
377 (a)
(Cyclopentadienyl anion)
This reaction is an example of electrophilic According to Huckel’s rule
addition reaction and in it addition takes Total number of 𝜋-electrons inside the ring
place according to Markownikoff’s rule. (4𝑛 + 2)𝜋electrons.
378 (c)
= (4 × 1 + 2) = 6𝜋 electrons
H2 SO4 absorbs ethene.
So, it is aromatic.
379 (d)
392 (a)
These all are poisonous gases.
Follow ozonolysis.
380 (d)
393 (c)
It is an anti-termite.
Natural gas is a mixture of 80% CH4 and 10%
381 (b)
C2 H6 +10% higher hydrocarbons.
The boiling points of straight chain or 𝑛-alkanes
394 (b) (i)Wurtz reaction
C2 H5 Br + 2Na + BrC2 H5 → C2 H5 C2 H5or𝑛-butane. Ether
2𝑅𝑋 + 2Na → 𝑅−𝑅
395 (c)
Alkane
According to Huckel’s rule an aromatic
(ii)Kolbe’s reaction
compound has (4𝑛 + 2)𝜋-electrons, where,
Electrolysis
𝑛 =0, 1, 2, 3,…etc. 𝑅COONa + H2 O → 𝑅−𝑅
alkane
(iii)Ulmann’s reaction
2C6 H5 I + 2Cu → C6 H5 − C6 H5
;4𝑛 + 2 = 2; 𝑛 = 0; aromatic
biphenyl
(iv)Frankland reaction
2𝑅𝑋 + Zn → 𝑅 − 𝑅
; 4𝑛 + 2 = 6; 𝑛 = 1; aromatic alkyl halide alkane
406 (c)
Both carbon have two sigma bonds on each.
407 (c)
; 4𝑛 + 2 = 4; 𝑛 = 0.5; non − aromatic
; 4𝑛 + 2 = 6; 𝑛 = 1; aromatic
397 (a)
Zn/H2 O
Alkanes with six to 10 carbons are converted to → CH3 − C − C − CH3
−H2 O2
aromatic hydrocarbons, 𝑒. g.,
|| ||
O O
408 (d)
Note this temperature used in oxy-acetylene
welding.
409 (b)
399 (b) Benzene can be obtained by heating benzoic
With acidic manganese dioxide or chromyl acid with sodalime.
chloride, in CCl4 solution, toluene and all other
homologues of benzene are oxidized to terminal
carbon atom giving aldehydes
402 (d)
All are dehydrating agents.
403 (a) Benzene can also be obtained by heating
Terminal alkynes give white ppt. with am. AgNO3
phenol with zinc dust.
404 (a)
Alkyl halides can be reduced to hydrocarbons
by means of Zn − Cu couple in presence of
alcohol.
Zn−Cu
C2 H5 I → C2 H6 + HI
C2 H5 OH
ethane 410 (d)
405 (d) Due to acidic hydrogen.
411 (b) 425 (a)
Fractional distillation of petroleum gives a large Chair form is more stable.
number of products aliphatic and aromatic. 426 (d)
413 (c) Both free radicals are used in terminating step.
𝑡. radicals are most readily formed. 427 (d)
414 (d) It involves removal of a molecule from substrate.
According to the Huckel rule, a compound will be 428 (a)
aromatic if compound should have (4𝜋 + 2)𝜋 Ozonolysis
CH ≡ CH → CHO. CHO
conjugated or delocalized electrons where 𝑛 is a Reduction
whole number and it may be 𝑛 = → CH2 OH. CH2 OH
0, 1, 2, 3, 4, 5, 6, … 429 (a)
It is a test for unsaturation in molecule.
430 (c)
On electrolysis of potassium salt of fumaric
415 (b) and maleic acid, ethyne gas is obtained.
CHCOOKCH
Electrolysis
|| → ||| + 2CO2 + 2KOH + H2
CHCOOKCH
Potassium maleateethyne
431 (a)
Column I Column II
Benzene (4𝑛 + 2)𝜋-
electrons
Ethylene Mustard gas
In this reaction H3 PO2 serves both as an acid
Acetaldehyde Silver mirror
as well as a reducing agent.
Chloroform Phosgene
416 (c) Benzene has 6𝜋-electrons, 𝑖. 𝑒., it follows
C2 Cl6 is artificial camphor.
Huckel rule (4𝑛 + 2)𝜋-electrons. Ethylene
418 (d)
reacts with S2 Cl2 to give mustard gas (war
1, 3-butadiene is CH2 = CH— CH = CH2; alternate
single and double bonds. gas).
419 (c)
Hexane and onwards alkanes are sulphonated. 433 (b)
Follow peroxide effect.
Isobutene is also sulphonated due to 3H-atom.
434 (b)
422 (b)
CH3 CH2 CH2 CH = CH2 + Br2
Acetylene has some acidic character and its
⟶ CH3 CH2 CH2 CHBrCH2 Br
hydrogen gets replaced by silver to give silver
∵70 g C5 H10 requires 160 g Br2
acetylide. 160×5
5g C5 H10 requires = 11.43g Br2
CH ≡ CH + 2AgNO3 + 2NH4 OH → 70
Ethanol
methanol
O3
(iv)(CH3 )2 C = C(CH3 )2 → Zn 523 (b)
H2 O
The structure of benzene is
CH3 COCH3 + CH3 COCH3 + ZnO
2 molecules of acetone
511 (c)
Alkynes are not found in free state due to their Bond order
high reactivity. number of bonds
512 (a) =
number of resonating structures
Least hindered rotation means free rotation, 𝑖. 𝑒.,
4
round a single bond. = = 1.33
513 (c) 3
HBr Since, the bond order is in between single and
H2 C = CH2 → CH3 − CH2 Br double bond, thus, it contains delocalised𝜋-
(X) bonds. Hence, it is not possible to obtain
Na2 CO3
Aq.KOH I2 excess number of single and double bonds in
→ CH3 − CH2 OH → CHI3 benzene.
(Y) (Z)
iodoform
515 (b)
In Wurtz reaction, an ether solution of an alkyl
halide is treated with sodium which removes the 524 (d)
halogen of alkyl halide and the two alkyl radicals −NO2 group withdraw electron from the ring
join together to form an alkane shows−𝑀 effect makes ring electron
517 (d) deficient, thus deactivates ring for
An immiscible and lighter substance with water electrophilic substitution.
will float over it.
525 (b)
518 (d)
Reaction of a non-terminal alkyne with a
These all are obtained from coal-tar.
solution of an alkali metal (usually
519 (b)
For 𝑡𝑟𝑎𝑛𝑠product we take Na/liquid NH3 or Li −
Na or Li or K) in liquid ammonia give
NH3 /C2 H5 OH or LiAlH4 as a reducing agnet (𝑎𝑛𝑡𝑖- a𝑡𝑟𝑎𝑛𝑠alkene.
Li⁄liq.NH3
addition) CH3 − C ≡ C − CH3 + 2[H] →
526 (d) 541 (d)
B.p. increases with increase in mol. Wt.
527 (b)
10. Benzene undergoes electrophilic Compound has 8 + 2 = 10𝜋 electrons
substitution in presence of
AlCl3 or FeCl3 or ZnCl2 .
hence is aromatic. has 4𝜋𝑒 − , has
11. Benzene does not undergo addition
reactions like alkene.
8𝜋𝑒 − , while has 8 + 1 = 9𝜋𝑒 − , hence all
H+
∴ C6 H6 + HOCl → no product and (b) is these species are not aromatic
correct answer. 542 (b)
It is a mixture of solid hydrocarbons.
528 (d) 543 (c)
C − Hbond energy is greatest in ethyne due to
the presence of triple bond.
529 (b)
CH3 — CH = CH— CH3is planer molecule due to
𝑠𝑝2 − 𝑠𝑝2-hybridised carbon atoms.
530 (a) This reaction is an example of Diel’s Alder
TEL increases the octane no. of gasoline. reaction
531 (d) 544 (d)
The refining of petroleum is distillation process. All of these can be used in cracking.
532 (b) 545 (b)
It is how Zn-Cu couple is used. General formula of a cycloalkaneis C𝑛 H2𝑛 .
533 (b) 546 (b)
CH3 — C ≡ C— CH3is linear and symmetrical and Toluene reacts with excess of Cl2 in presence
thus, dipole moment is zero. of sunlight, the last product of this reaction is
535 (a) benzotrichloride which on hydrolysis gives
𝑅COONa ⟶ 𝑅— 𝑅 + 2CO2 + 2NaOH + H2
benzoic acid, and it gives sodium benzoate on
537 (b)
reaction with NaOH.
Only terminal alkynes give precipitate with
ammoniacal silver nitrate solution.
Among the given, CH3 − C ≡ CH − CH3 is not
a terminal alkyne. Thus, it does not give
precipitate with ammoniacalAgNO3 .
539 (c)
Benzene vapours mixed with air when passed
over V2 O5 catalyst at 775 K gives maleic
anhydride
548 (d)
CH3 CH2 COOH + NaHCO3
540 (a) ⟶ CH3 CH2 COONa + H2 O + CO2
2CH3 CH2 CH2 COONa → 549 (a)
Anode Cathode 5
⏞
C2 H2 + O2 ⟶ 2CO2 + H2 O; 1 mole or 1 vol. of
CH3 CH2 CH2CH2 CH2 CH3 +2CO2 ⏞
+2NaOH+H2 2
C2 H2 requires 2.5 mole or 2.5 vol. of O2 .
550 (a) compounds.
Conjugate dienesare mores stable than the other O3
CH3 CH = CH2 → CH3 CHO + HCHO
dienes. H2 O 2
551 (c) Acetaldehyde formaldehyde
Branched chain alkanes give rise to increase on 560 (a)
octane no. Petrol or gasoline contains mainly C6 to C11 atoms
552 (d) liquid alkanes.
Follow Markownikoff’s rule. 562 (d)
553 (b) L.P.G. mainly contains butane and isobutane.
HOCl has Cl+ and OH − ions 564 (a)
[O]
CH2 = CH2 → 2HCOOH
565 (a)
554 (b) According to Markownikoff’s rule, the
negative part of the reagent gets attached to
that double bonded carbon atom which has
least number of H-atoms. Thus,
HBr
Zn − H2 Ois the reagent for reductive work up CH3 = CH − CH3 → CH3 − CH − CH3
of ozonide. H2 O2 − CH3 COOHwould give |
HOOC − (CH2 )4 − COOH. Br
555 (d) 569 (b)
The 𝜋-bond is unshared in electromeric effect to Gasoline contains alkanes from C6 to C11 carbon
give+ve and –vecentres on molecule. atom.
570 (d)
We know that,
556 (d)
Al4 C3 + 12H2 O → 4Al(OH)3 + 3CH4
Thus, in this reaction methane (CH4 ) is
produced.
Tropyliumcation is planar and have 571 (d)
6𝜋-electron according to Huckel rule, hence it Follow Saytzeff rule of elimination.
is aromatic. 573 (b)
Impurities of PH3 give garlic smell to C2 H2 .
574 (d)
In the formation of an alkane from Grignard
Cyclopentadienyl anion is planar and
reagent, alkyl group always comes from
have 6𝜋-electron, hence it is also aromatic
Grignard reagent. Hence, the number of
compound.
557 (a) carbon atoms in the Grignard reagent and
Follow peroxide effect. alkane formed Grignard reagent will be
558 (a) identical. So, the original alkyl halide is propyl
In the laboratory, nitrobenzene is prepared by bromide.
nitration of benzene with the mixture of nitric 575 (c)
acid and sulphuric acid at temperature
below60℃. In which HNO3 acts as a base
559 (d) CH2 = C(OH)CH3 ⇌ CH3 COCH3;
The reaction is ozonolysis. During the The mechanism involves tautomerism.
reaction C = C breaks to give carbonyl 576 (d)
7 C4 H6 may contains either two double bond or
C2 H6 + O2 ⟶ 2CO2 + 3H2 O
2 triple bond
577 (c) CH2 = CH − CH = CH2 orCH3 − CH2 − C ≡ CH
HBr HBr
CH ≡ CH → CHBr = CH2 → 590 (b)
KOH(alc.) NaNH2 Due to acidic—H-atom propyne forms CH3 — C ≡
CHBr2 — CH3 → CHBr = CH2 → CH ≡ CH
CNa with Na.
578 (d)
591 (b)
According to Markownikoff’s rule the
More is b.p. lesser is volatile nature.
addition of a reagent (HX) to an 592 (d)
unsymmetrical alkene takes place in such a These all are used to increase octane number of
way that the negative part of the reagent will fuel.
be attached to that carbon atom which 594 (a)
contains lesser number of H-atom. CH2 = C = CH2;
Br 𝑠𝑝2 𝑠𝑝𝑠𝑝2
| 600 (b)
CH3 − C = CH2 + HBr → CH3 − C − CH3 Benzene undergoes electrophilic substitution
| | reaction. It is nitrated by HNO3 .
CH3 CH3
2-methylpropene
579 (b)
Follow text.
602 (b)
580 (a)
Markownikoff’s rule is for addition of
Br2 solution is decolourized by alkene or alkyne or
unsymmetrical additive on unsymmetrical alkene.
molecules having unsaturation.
603 (d)
581 (c)
Paraffin wax are solid hydrocarbons from C20 to
Eqs. (i) and (ii) drawings are Sawhorse and
C30 atoms.
Newman projections respectively for staggered
605 (d)
forms.
Methane is called marsh gas because it is
582 (a)
found in swamps or marshy places and can be
C2 H2 gives white ppt. with amm. AgNO3 .
583 (b) obtained by bacterial decomposition of fossils
Oxidation NaOH of plants and animals.
C6 H5 CH3 → C6 H5 . COOH → 606 (b)
(𝐴) Among hydrocarbons, alkynes are easily oxidised.
Soda lime
(NaOH+CaO) 607 (d)
C6 H5 COONa → C6 H6 + CO2 ↑ B.P. change with branching.
(𝐵) 608 (f)
585 (c) These are few oxidants.
Cyclobutadiene have (4π) conjugated or 609 (a)
delocalized electrons, thus it is 𝑎𝑛𝑡𝑖-aromatic The acidic character of H is,
586 (a) F— H > 𝑂— 𝐻 >≡ C — H > 𝑁— 𝐻; H-atom
sp
HOCl
CH ≡ CH → Cl2 CHCHO attached on F, O, N and triply bonded carbon is
587 (c) acidic.
Thioalcohol (mercaptons) have unpleasant odour; 610 (b)
C2 H5 SH is commonly used. H2 /Pd
CH3 CH2 CH = CH2 → CH3 CH2 CH2 CH3 .
588 (c)
611 (c)
Octane no. of triptane or 2,3,3-
Except acetylene, all terminal alkynes have only
trimethylbutane=124; octane no. of 𝑛-
one acidic H-atom.
nonane=−45.
613 (d)
589 (d)
Alc.KOH Amm.Cu2 Cl2
C3 H6 Cl2 → CH3 C ≡ CH → CH3 C
≡ CCu ↓
red
These compounds are known as epoxy ethane or
oxirane or cyclic ethers. ppt.
614 (b) Compound (𝑋) gives an aldehyde when reacts
According to X-ray analysis all carbon-carbon with aqueous KOH. This suggests that both
bond distance (1.397Å) are equal in benzene. the halogens are present on same terminal
The bond order of carbon-carbon bond is 1.5 carbon atom. Thus, the formula of compound
in benzene. (𝑋) is
Hence, carbon-carbon bond distance
(1.397Å) is less than C − C single bond
(1.54Å) and more than C = C double and the reactions are as
bond(1.33Å). follows
615 (c)
Cracking involves decomposition of higher
alkanes to lower one on heating.
616 (a) Ammoniacal
CH3 C ≡ CH → CH3 C ≡ CCu ↓
Follow mechanism of Wurtz reaction. Cu2 Cl2
638 (c)
In benzene all the six carbon atoms are 𝑠𝑝2
hybridised. Out of these three 𝑠𝑝2 hybrid
orbitals of each C-atom, two orbitals overlap
with 𝑠𝑝2 hybrid orbitals of adjacent C-atoms 649 (a)
A method used during II world war.
to form six C − C single bonds. The remaining
650 (d)
𝑠𝑝2 orbital of each C-atom overlaps with 𝑠-
Ozonolysis of these two produces different
orbitals of each H-atom to form six C − H products.
single sigma bonds. Each C-atom is now left 652 (c)
with one unhybridised𝑝-orbital For simplest alkyne 𝑛=2; thus, alkyne is
perpendicular to the plane of the ring. C𝑛 H2𝑛−2 or C2 H2.
640 (b)
654 (d)
Alkene is CH3 CH = CHCH3, a symmetrical alkene and therefore alcohol is,
655 (b)
Cyclodecapentaene and Cyclooctatetraene both
are nonaromatic. Cyclobutadiene is antiaromatic
while benzene having 6𝜋-electrons is aromatic
656 (d)
CH3 CH2 CH2 CH2 CH2 CH3 ;
(CH3 )2 CHCH2 CH2 CH3 ;
CH3 CH2 CH(CH3 )CH2 CH3;
(CH3 )3 CCH2 CH3 ; (CH3 )2 CHCH(CH3 )2
657 (f)
These are facts about alkanes.
658 (c)
Due to resonance, benzene is quite stable and
inspite of three double bonds does not ∴ C2 H4 (an alkene) reacts with KMnO4 and
decolouriseBr2 water.
decolourises it and does not react with
659 (c)
AgNO3 , C2 H6 and CH4 are alkane they do not
Follow peroxide effect.
react with KMnO4 and NaOH.
660 (d)
663 (c)
The reaction is Wurtz’s type reaction.
It has maximum octane no.
664 (c)
Pure C2 H2 has ethereal odour.
666 (a)
661 (a) Alkylated alkenes are more stable. More the
Alkynes give different products with alkylation of alkene, more will be its stability.
different reducing agents 𝑒. 𝑔., with Lindlar’s ∴ Order of stability of alkenes is
catalyst (Pd⁄BaSO4 )or Ni 𝑐𝑖𝑠-alkene is 𝑅2 C = C𝑅2 > 𝑅2 C = CH𝑅 > 𝑅2 C = CH2
formed but with Na in liquid NH3 (Birch > 𝑅CH = CH2 > 𝐶H2 = CH2
reduction) 𝑡𝑟𝑎𝑛𝑠 alkene is formed. ∴ Tetra alkylated alkene is most stable.
668 (d)
CH2 = CH − O − CH3
HBr
→ CH3 − CH − O − CH3
|
Br
First protonation occurs, two possible
662 (c) intermediates are
(i)Alkene and alkynes both react with KMnO4
and decolourise it.
(ii)Only alkynes react with AgNO3 to give
white precipitate.
II, is more favourable. Hence, Br − attacks, and
product is
CH3 − CH − O − CH3
|
Br 678 (c)
An alkyne has higher b.p. than corresponding
670 (b)
alkene and an alkene has higher b.p. than
Halogenation of benzene in cold and dark is
corresponding alkane.
carried by electrophilic substitution. In this
681 (d)
reaction, Cl+ electrophile takes part in the
On ozonolysis,
reaction.
CH3
|
CH2 = C = C − CH = CH2 gives two moles of
HCHO, one mole of CO2 one mole of
CH3 COCHO.
AlCl3 + Cl − Cl ⟶ Cl+ + AlCl−
4 CH3
electrophile |
671 (a) O3 ⁄H2 O
CH2 = C = C − CH = CH2 →
Since the alkadiene on reductive ozonolysis Zn
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