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    Identification Questions Organic Chemistry Class 12

    Uploaded by

    Kalyani Kolpe
    The document discusses the reactions and identification of several organic compounds based on their reactions and molecular formulas. Key details include: - Alkene A undergoes ozonolysis to form carbonyl compounds B and C, which can be identified by their reactions. - Isomers A, B, and C are carbonyl compounds that can be identified by their reactions with Tollens' reagent and iodoform test. - Aromatic compound A is identified based on its reactions with DNP, iodoform, Tollens', and bromine water. - Compounds A, B, and C are identified and their reactions described based on molecular formula and reactions with reagents. - Is

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    Identification Questions Organic Chemistry Class 12

    Uploaded by

    Kalyani Kolpe
    332 views2 pages
    The document discusses the reactions and identification of several organic compounds based on their reactions and molecular formulas. Key details include: - Alkene A undergoes ozonolysis to form carbonyl compounds B and C, which can be identified by their reactions. - Isomers A, B, and C are carbonyl compounds that can be identified by their reactions with Tollens' reagent and iodoform test. - Aromatic compound A is identified based on its reactions with DNP, iodoform, Tollens', and bromine water. - Compounds A, B, and C are identified and their reactions described based on molecular formula and reactions with reagents. - Is

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    The document discusses the reactions and identification of several organic compounds based on their reactions and molecular formulas. Key details include: - Alkene A undergoes ozonolysis to form carbonyl compounds B and C, which can be identified by their reactions. - Isomers A, B, and C are carbonyl compounds that can be identified by their reactions with Tollens' reagent and iodoform test. - Aromatic compound A is identified based on its reactions with DNP, iodoform, Tollens', and bromine water. - Compounds A, B, and C are identified and their reactions described based on molecular formula and reactions with reagents. - Is

    Copyright:

    © All Rights Reserved
    Download as DOCX, PDF, TXT or read online from Scribd
    Download as docx, pdf, or txt
    332 views2 pages

    Identification Questions Organic Chemistry Class 12

    Uploaded by

    Kalyani Kolpe
    The document discusses the reactions and identification of several organic compounds based on their reactions and molecular formulas. Key details include: - Alkene A undergoes ozonolysis to form carbonyl compounds B and C, which can be identified by their reactions. - Isomers A, B, and C are carbonyl compounds that can be identified by their reactions with Tollens' reagent and iodoform test. - Aromatic compound A is identified based on its reactions with DNP, iodoform, Tollens', and bromine water. - Compounds A, B, and C are identified and their reactions described based on molecular formula and reactions with reagents. - Is

    Copyright:

    © All Rights Reserved
    Download as DOCX, PDF, TXT or read online from Scribd
    Download as docx, pdf, or txt
    of 2

    An alkene ‘A’ (Mol. formula C5H10) on ozonolysis gives a mixture of two compounds ‘B’ and ‘C’.

    Compound ‘B’ gives positive Fehling’s test and also forms iodoform on treatment with I2 and NaOH.
    Compound ‘C’ does not give Fehling’s test but forms iodoform. Identify the compounds A, B and C.
    Write the reaction for ozonolysis and formation of iodoform from B and C.

    (A), (B) and (C) are three non-cyclic functional isomers of a carbonyl compound with molecular
    formula C4H8O. Isomers (A) and (C) give positive Tollens’ test whereas isomer (B) does not give
    Tollens’ test but gives positive Iodoform test. Isomers (A) and (B) on reduction with Zn(Hg)/conc. HCl
    give the same product (D). (i) Write the structures of (A), (B), (C) and (D). (ii) Out of (A), (B) and (C)
    isomers, which one is least reactive towards addition of HCN ?

    An aromatic organic compound ‘A’ with molecular formula C8H8O gives positive DNP and iodoform
    tests. It neither reduces Tollens’ reagent nor does it decolourise bromine water. Write the structure
    of ‘A’

    An organic compound (A) having molecular formula C4H8O gives orange red precipitate with 2, 4-
    DNP reagent. It does not reduce Tollens’ reagent but gives yellow precipitate of iodoform on heating
    with NaOH and I2. Compound (A) on reduction with NaBH4 gives compound (B) which undergoes
    dehydration reaction on heating with conc. H2SO4 to form compound (C). Compound (C) on
    ozonolysis gives two molecules of ethanal. Identify (A), (B) and (C) and write their structures. Write
    the reactions of compound (A) with (i) NaOH/I2 and (ii) NaBH4.

    A and B are two functional isomers of compound C3H6O. On heating with NaOH and I2, isomer B
    forms yellow precipitate of iodoform whereas isomer A does not form any precipitate. Write the
    formulae of A and B

    An aromatic compound ‘A’ on heating with Br2 and KOH forms a compound ‘B’ of molecular formula
    C6H7N which on reacting with CHCl3 and alcoholic KOH produces a foul smelling compound ‘C’.
    Write the structure and IUPAC names of compound A, B and C.
    An organic compound A’ with molecular formula C7H7NO reacts with Br2/aq. KOH to give
    compound B’, which upon reaction with NaNO2 & HCl at 0°C gives C’. Compound C’ on heating with
    CH3CH2OH gives a hydrocarbon D’. Compound B’ on further reaction with Br2 water gives white
    precipitate of compound E’. Identify the compound A, B, C, D & E; also justify your answer by giving
    relevant chemical equations

    An aromatic compound ‘A’ on treatment with aqueous ammonia and heating forms compound ‘B’
    which on heating with Br2 and KOH forms a compound ‘C’ of molecular formula C6H7N. Write the
    structures and IUPAC names of compounds A, B and C.

    An organic aromatic compound ‘A‘ with the molecular formula C6H7N is sparingly soluble in water.
    ‘A’ on treatment with dil HCl gives a water soluble compound ‘B’. ‘A’ also reacts with chloroform in
    presence of alcoholic KOH to form an obnoxious smelling compound ‘C’. ‘A’ reacts with benzene
    sulhponyl chloride to form and alkali soluble compound ‘D’. ‘A’ reacts with NaNO2 and HCl to form a
    compound ‘E’ which on reaction with phenol forms an orange dye ‘F’. Elucidate the structures of the
    organic compounds from ‘A’ to ‘F’

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