Chemistry Notes
Chemistry Notes
ouds:
Uosi cati'on
hain)
NH coNHa Acy cic, (open
aulphate
amnlnn
y a n s e
Aructral Rephesentotion :
"Tuan otane ’ C3oH62
comp e th Pep
oLpo may or
n-¢--H
Gec- Butyl
conellnsed fosm
sbsttuled
"hasn-wedge eorver)
daat (auay fron nisile
c on koot
’ spou ng
hyorony ud ketones.
enplained e t i e ize
eachaOm boeo
On vodswoals.Baius. X
E %actual
esngy Resena
canbanon (ag)
0slnanee
L distor ed
4etohedn Ressuance is patIlan mportent
sen te ordiauting a c t e r e
a mo e ugecben s
hawe
nucer
>tame n o wpared elactrns.
u+ & Pplaty pbduceol n He malale ley
cdjaen atom.
cange
dipaig te postio
bord, as peAsesstng
parta oie uas cue to ngonenet
tacke ypercjgatrow
Hydso abans
Coal a,iu obtained by te destuctie
distiation e coal
40meretian: ounh
n-nenane
HU.
Crs0s/_0s/Mo,o3
(Mean)
Sindstrial pmeparatm t
euolvea He Pmin ape JRCacR'**
Pyeyhi.
this ia paaoised
deactivnaed
ancsa pastaly
otth eosens se
Paptoue Petene suphh comp Qunde euinoline gie
onsttuent
akenes. (indland's cata ny t)
aleshoc KOH eliminedes 'a
osd te tesnuelen aawh thet is uehyy Rae ' ' > j "
dstubed detó hatotn.
bt
wder
->Ahenos welergo aold dorgo
con ometimes
speua cong
free ra'caA Sibe
I-20k3/mol d e t o weak hepuls Ons
blwtte,
A NkR Add mehe
teyellelar'aUC
couisens
t has not been possie to epak dtt
ontormational isoneers , eHant yet
gies an iy ciiud.nell
weake n- bend aks
aUkenee ntable n omposson to "Polyphopeis needastctorbagse oud
nenugature
mik Gates aer
wmoded a h l e s
L0ninal agei*
Gut
cs sonrérens (dl to dipe)
pt ) tens is (Racr)
ALKYNES AROM tiC HYDRO CARBONS
eAyne (Aceyleug) caled arenes ( ° e s s Peas at
oolow)
L»aed mahe welong
ber m oyacetylene t&me "fosn
tio2ewele hol'cated
Ovteibuting sthuctes
ntehmla aux. "There is egual pobaoility ter the
p-erb tak o eah coabQ to eerep
PQuiCine) oith tte ay p-6rbi'tel .fer n bgndp.
This ccn be gepheaented by dghnet
OT +N
Phgdiat
pe
9Theonyt cheide -pngend Bhomae ineided p olo
whn
Gnng pne alyl beide.
ae
gao at eem tyo.
3°alueols -umely chaling
ee tu at ngem
tmp. intmeuen
(dipoe - fouo of atratin
n) owtant oling witn Her(487) clipole, Vun dur wealo) Canbon
holoopeundo. steng
q57. hophephnis id.
brncuing.
Mpt: P>0>m
dittiatt clanor
bctionef doute bend : 9Jpuale in H, o (E %g wied te
attraten blw moie to eon
cly, 4-bondo blwiuhalo allee meles beak
+ Maddisn cueing new
wene than tue E elensd
Cutractien)
Fincelettn
R-x + NaI ds,
oUtone RI + Nad/Br KCN RN ( mene ieni
both CNcen
ddente beceUee
KNO, R-o- NeodMhesn
in he te
failitat in RNo
forwerd pH
Swartz RR'
R-x + Agf SN 2nd oroln winets
RF + Ax SN
Dowi
) phy c-c stase
Naoh, 23 K OH
300 am
Ht
feyhalogew
9 Muylene
ompound dipluryt
di heit, cleids CH, u.: am
sn contact hnam Ns
Diguct
intene bni
ntac wiheo can
Notes
Protorated alcokols as eletphiles
NaoH
they react as eletiophiles.
hhO4 +
3 CH
ntacten, aleohol Bn e****c**.
In tu yied.
obtained in eaccellent
R- HO+ H
ane bronates
açido , ie, they cam donate a protn
ty to a a b s n n base.
ercellent yield k
in
atrony eduey Bcidie chasacter eleohol iscdue
to the polar natuhe y o-H bond.
eageut &thete e gpeielemicals fodium ethontde, la a abengu
acds
"Cosmnecially, audo ara reduj bae tha oodium gduentd
accegar them lydmide lem
to eatone folowes bytheet redut hgrideo anethsnger bae
tham golnoude
atalyatlonblytiebydroge)
Meeelo at a brenstes bases as
atkyR-HOH uell.t io dee to t e tne ot
whieh alees tein prten acpta
oleu
he reaction e! phenol wutth aaueo
odiun tuydroaide lindicates that
phts are stonge aldo tan
-Diagonium salta are bydroyaed alohols uater
by trety cuith dilce aeld. thogh there ia albo chage
deloalatin in phnol, io ionane
aide
takes plae & amnne
3* CHyLOH
S73k
colewr
melling pnidine Ca Paet
qudj.
devtition f aliohol.
HaSoy
CH,
443k niroe mdorgee bilgmination
with boomine n ethanoc a
413K
ore.ot
a el. 7hey eat
elimim balido lehdiy to
Miaceulity of etheu with wator
9esembls thee 9falesho
e e molealar masa
Stthe are e leant reatiue
Te eagefmctigmal g
cobsus in ethe
taleo
goge laidea
TROR+HX R-X+RoH
Teden e! ractiuity HXo
IHer>Ha. lenge et
aees_lace cth cgne HI
CAR BONYL COMAOUND
DATE
DATE:
"attomam koch na
eetas B ketas ane Motes
menel aue
wth aa
Bapt'o aldehyde &kebone Co, Hcl
cHO
by deluydrghalsgenatqae. gdeyde
ketones
d ammenia s deintin
aeytcloride
In tie methad alohayse " Brep ketee poom
2Rmgt+d cl
admiun
’Rcd +2y)u
ike (g .
Eaprodnt
+&d
dalkye formatdue be intenmedit
HO. admin hapid denydrat ofthe
Palasoy cderocpmate
Jtophen sen
R c tSnartHU’ R-4>NH -Hho
Jsot
R-CHO ketgme merethan aldelyde
DIBAL-H ompable mas.
Tallens teat foadehyckke
scew in alkalne edim.
ith P t HCN. it
DIBALH doonet rede dgube bonde gemerates + 30H
*bsz Brep gm Hc wsiny comy a atherger
compsmdo"a0 uconayoonding
hetie Fehlings teetNet piga
yemohyoli temediate fetiny ticu soy
8 : sdimpetasium
JHsot tartate(louheles
alt)
Bath are taean ineuat amt
mid befse ast
Bgund
a R-HO 2cu 2tSON
taiin),
deeti Positisn oeanlibium
anhyd. Ppt.
Hs ot Mgat ketgnee : Left ide
aniyyano n dusprep
eakbngaldodeThia
gmmeeal meto he
mamfolure
bmgaldehyde JOR
g'oH
HU gad
otes
C"Acids
The
DATE:
alohole tá a tind o
nueleeplilii aey mubiitution .
gones eageut: Cho -Has0y
Gidiats 1ale ’anboyie aid
Prep trom alley bemsene temg
kmako que amide
4NHs
o0NHyt
nmeium
im th mamewlile tebiang grup hthalete.
io ngt atteeted.
Sitably Subatttted aiknes are Phthalimide phthaeide
aleo idicdto ctdo witth then
deanitiony ledut e Chida
ROOHAenCOtahalehen K-h
H3ot
R-CN o A
R-cOcL OM-/QRoga0R-ooH
oMene eadily hydrelysed uth
*****
Henan dote tt wg
dhydntde tthe
kMnou
kon
CooK
Knoy
Quarteay angiim
L
salla ’suitatanto
lyobel ethalinide rymthesi
*arat"ot 1°amie
for tuinmethyl ammine loe amns camnst be prinag
eporred
alkytlary t i method because aryl haldeo
3
do nat wndergo eletphiie
sin mines ainesi ditteret greyo ubattut neat with ien
tamed by pthalmide.
Regu
CH3NH methanamine e t
alkeae
Hott Bruomide begadatn
-,2-diamine R-NH t Br t 4naH
R-NH t wa3tlasrt 2Hh0
thuilene asth comnon &tUPAe namme contiye
len than
eos ansemyta
anie renoue as co32
J,tUPAC name
bnyenamine e' 2ene
be
emoved. Preparat"ot runmary amineo
No
fetHL
thene?
ugution ot an alkyl an
eeterel becawe fel fomed gek ag op takya plae from
carbon of aiae to tii nibioge
gdrsyes toreleae Hei ouriny atom.
Motes DATE:
N-Ce Hs+ Hl
trongyaie
N-ethyt benyeneushonanide
2amine (aoliblenalkoli )e jenealy slores &is waes
+ 4-NHr
immediely ofter ito prepanat
. .
CeHs Nu>colouless
Lredbyeoluble iner
(N,RNo p h o n e m i d e )
lacto with warwlhen
wared.
beegmpgeo
3 amme domt neat wuth eany im dg atata,
bengeneauphonyl
leide. Bemgene diagenun fueobraa
io wiatr insstublo &taklaot
dhee day, bengeneutheng
celeide io seplaced og
p-totnelphomgl chloide An
aucnKcNrcN +N
NH
+3HB ulH >Ara +Ntux lyotten
en
iept
be aettes tham fiattema kertie
To tode igdine
yridia A N a t k I ’ A r I tku+N
Toitodue Rusine
NaNO
ol+N,tNagfy
Onge dye
Coupliy ahenol
Begenee Oh
p-ydrory ayobengeme
diasenim
hlorideaalt
aniliie
anemnatelgnp
pupares by dirat eubetitatijnot
bengene btetted bemsene
>Asaeien PERIODI C PROPERTIE S
Scientist Jea
Johann bobereinen 182 4 lam ot Toiads
la’HO u’ 35 5 Avg m biamises a
PY
lemeut
Element donn thegß
IE 2EN deeeseo
1t Ienioatiem Enegy
mept
Te >se > S>o
B> T > 4a>Aln Polymenle etalic
But m the 2d IE (ergthemi)
|Prefo af ydrides
m-pt &Bept
H0> H Te > H te >Hs
Elenonegaliity Tl
& bond agle
m eases
benddength
A we go den the gro, dleneases
-Denaiy Amlaseg
e gÕ dewnte nadius, lnioatg enthaby
No encetien
Bpt dewrlane as we &Eletiomegaluity
go denn the gt
meltig foint due to IPE Electren gain emthalby
E°ae ot TL/TL- e F= -333
>FBr>I
for , ya, ln, Tlz+ue
Br -2 25
I - -296
Bept
Mpt
HEH amge formeN-H bemd
M2t /M
T
Mn