Hydrocarbons- Complete Handwritten Note, Summaries of Chemistry

This version of my handwritten notes includes the whole of hydrocarbons in the most basic detail. It goes basic topics in hydrocarbon like Alkanes(isomerism, methods of preparation, physical properties, chemical properties ,reactions of alkanes, projectile formulae and conformations, Bayer's strain theory of cycloalkanes), Alkenes(isomerism(including geometrical isomerism), methods of preparation, physical properties, chemical properties, reactions of alkenes), Alkynes(isomerism, methods of preparation, physical properties, chemical properties) and Aromatic Hydrocarbons(aromaticity, preparation of benzene, physical properties, chemical properties, directive influence of functional groups in mono substituted benzene, carcinogenicity and toxicity).

Typology: Summaries

2023/2024

Available from 08/22/2024

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bg1
Hyhocanb
rlal
els
fachooal
\mportnt
coal
Bo
LNa
AL
LANES
’ALKanes
hde
comP
hane.
aY
ydo
cabons
ae
ctassified
n te
Sarated
c sinalebonc
onl
-alkaM
are
ey
ne
-
Owiatotcl
Csinglemlh
onli) -alkeney yalkyho
-onatie
’Siet
H
HYDROCARBoNS
Comound
ofCqrbon
bydyon
ory.
lselç
beause
of
t
ieh
com
riqiliby(eo
tamic)
dishllatio
’general Y
mula
-Cntz0
42
cru
de
ol
ule
al
ga,
aoher
(uol S
oslaned
y
decfue
distilati
Sp3
H
CM4
ane
move
e
ien
-el
ii
leaS
poluin
blcined
fom
dfer
y
alkao2
normal
conhbns.
tetra hedel
104°2
'
knuwn
Akanu
ormomoluqous
Seles
5
me
nane (Ctu-
marrh
ges)
les
elechonogatie.
loeaty
rle
CAR
Bo
AGMS:
any
ono
ocegenk
Succe
se
pf3
pf4
pf5
pf8
pf9
pfa
pfd
pfe
pff
pf12
pf13
pf14
pf15
pf16
pf17
pf18
pf19
pf1a
pf1b
pf1c
pf1d
pf1e
pf1f
pf20
pf21
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pf24

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Hyhocanb

rlal els

fachooal

\mportnt

coal

Bo

LNa

AL LANES

’ALKanes

hde

comP hane.

aY

ydo cabons ae ctassified n te

Sarated c sinalebonc onl -alkaM

are

ey ne

  • Owiatotcl Csinglemlh onli) - alkeney yalkyho

-onatie

’Siet

H

HYDROCARBoNS

Comound ofCqrbon bydyon ory.

lselç

beause of t ieh com riqiliby(eotamic)

dishllatio

’general Ymula - Cntz0 42

cru de ol ule al ga, aoher

(uol S

oslaned

y

decfue

distilati

Sp3 H

CM

ane

move e

ien

-el

ii

leaS

poluin

blcined fom

dfer y

alkao

normal conhbns.

tetra hedel

knuwn

Akanu ormomoluqous Seles

5 me

nane

(Ctu- marrh ges)

les elechonogatie.

loeaty rle

CAR Bo AGMS:

any ono ocegenk

Succe se

acH3-c-cM -CH-H

I50 MERISM

A\Kans Can

Akane

H

Akan can abo r ibit dere o150mensn

comfatbnal 1somerism

de+)

non no

MEtHopS of

becau Se

Baned

H

Say

show tructual honansn Sueb a Chony pasios

hial

meta Sorfue e

I'H

2°H 2

)

ftom

unsatuated budo

caybons

(heen

a

AkynS)

Carban (omymeie cew bon.

PREPE RATon

Catalytie yyoqonaion (s

stati by

a |len

Sune sidatteck

addu ttn

H -C

cH

nat

alkyn1 toweney olecopie

CH,CH, CA

Y2actEive

addith.

gonton.

funme

CH1)

C arbo cat

iwtatiwn:

  • Wtz vxn
bez ule

CH3cl t cHg cH, c

)franklanc rxn

Me

Mane

canno

(

lae ve

par ed

2 R-X

Reagent

PYep

Cave

(9) CoYeu-House nneS)s

LiKe

be

Na

dry mer

Br

d.e

USedn

nbn as

Dialkyl Litbium

Cupyaie (R

Cu Li)"

iilaann's reOgeht

of Gilmaws Yeagont

ighor alkane ajny.

een

Noy low

dry etmey

(CH3),Ci ~

alkane pralirod but

cHs

ore

alkee

y hase Sylhess

mehne ( (Hy)

|) Vsing aignard teayent

RX

(a)

Socla

imedecanoxy

lation

Nech

(b) Kobe's

At

CHg Co Na

polar ptte

SoWents

CH 3CH, (Hy Coonla

2 CHz -

C. a.

2 Ctl3 -

(lectolys is

42H,

anode C0n).

alhene

At atn ode (red):

Ca O

CHu

elee tolyis

2 CH3 - -o

2 CH 2

H+ H > H,

4 Na C0g.

t 2

+2602 t

Gubshhtion takes pl<ce.

tbey

substae cootin bae senste 4ps

leaVe

Pysical prpetteli

sshong

As

Som tne

ton

curechu cattached

Prin ple. alhans

() Mihing point

enen no.

)\kasesr areamus t

gènenally

e Do:

OH

carbon aton, Ci-Cy qee

CH

polar

bez

o

esall

eleco

uka dssolu

ane

mre

Sowble in

non- pol

solWent

afc atoms

of

e

tiaa

poinl

nalsg ns

oy si alkanS regulo,

(kany

Gughty

il

than

th a

BP

1

branehing

contzei

CHy

Cnemlcal pphes

(() Suostitutoo YXrn

No' of

ALkaney

uodeo

sfiton

xn

Such

hAolecules becone miste

which

CHa

lower

a

lka

doen

sno

man

y

Sulphont,tut

m

all

alkany

oxiibit

balgonatun

halsgonaion s

-cH, - cH - CHg

cHa

H

yteolect ay fovee sB.

roo0ooroodicts

ientl

Q) hydgen.

3'H7 2°H>1°H

o halgenatn,

FaC,> Bra

bcz tabiuy order

J

= no: f cieren

tye otcatwy

cartainy at lent

hyduen

CHs t1,CHg+ tHJ

SHI tHTO, ’31,

ntetion

so relasilble

fcaciitle frw

yM

Ophcal iSen

3°>2°>1°

No.

ot

wouocwo

pets

oclucing

steveoisoe

o( free radicah

)24g-cag

CH)

CH,3°H

Alkane

underqo

soMe|satntofom1s0mers

in

presonle

f

nhy dous

)extion

A\kene

lkane baing

Unday

auwy

ACs

cHa

CH

cHo- CH

-CH

|HC

Akane

hawing

no.

ot

c

atow

to

Und A

aud dehydyenalon

CMo,3,Crz

os)

up

ported

bn

CH

CHg-CH

y 0- 20 at

iib team

143k/o - 20 atm

1213k

-CH -Cty-C3 t3.

443L-20atn

) Pyrolyeis

(Crackny )

Hiqher aWan

Unde

high temperie prodxe

PresS0re

Pocces

benene

u ts

danuate).

steum

greater han Yeqal

Ner

Co t 3Ha

(A;03) Awina

undarqo cycusa

n Presonce ofNi

neat
Gobjected t
amstkt

car bon kuon

wËonemts

ot

hyd

cay

horizontal ichinaupscna

benindte,al

unn erti cala

tl

ich

F

Tbr epreyontetin

inudli

-to iney

Cowponets

at ol

Varhcal(ne goPS

æ)

Solid-

dahJedga

Yepresentasi

can be repe sonte t ovon

f applied,ne of podutnoil y

C3Hio tGHytCtly.

tl t2tl

(") Fsebay Prjeto

l

Urganic molecuen

PROJECTION foRoLAE

Plane

be

tHe AkSCotn

beptane

can Polys1s

Crackny

eeipse d eutywatun

H

H

H

H

echspseA

H

H

staggo1ed

staiihy: stagend> eacipsd

H

CH

Sp 3.

Accodvy te Bayr

H

bayer s

straun

theowy

for

cuplsalkaner

a

CH

H

CHlg

WAolecule

auele sten

from

woywal

hedal amale

of

HH

deiation

\0 28!

(noima\angle -

ooue

angl)

Hy

loond anls

I(n2120)

A

S-A

loA"e-

qo)

I

Stab ordey 5>0>473..

c can

Stlay

Zxpeime

ntally

cuclo

loxau

s

islay

stae

Thon

cplo

pete

be

deteuisy

ts

eonfonal

anass.

ALKENES

0.5°

chair : tisted bt lat Halt ha

o-8) -12))

genral fomula: CnHn

SeñeS

generalhy Muon

H

H

TDe hae thaqonal planor

tplanv

S -33.

|SoMeMsme

6>5>s

aleehnoge

(wss

Alkenes

enes eua

OleteA 2 ft mow bey ehene

meubey

thay a\kane.

stucue IoonerIsm

A\kene can aso ezubt

Sucu ay

iing

cha

METH0ps of PrERERALoN

fom Alkynes (catalyte hyogenai)

2

eagerts.

Ha t rdlc pavtially possoss iheor Qoirdone

i) H, t

Na/Liq NHs

et.

i)

CH=CH

tHg

  1. CHa-C=cH

  2. cHrcEC-CHs

uFow Alkyl Hald

ndla Peagent

eliwunah on

H

Cxcwsive

iy

predLg

than alkene.

J0)t-Çi-cHs

axc sively

CHs-n =cHz

Akyl Haides ondovo deydo hodogena by haatne 1t

deponcng opanthe rxn cond n

alkone. ica

cuocoa)

tertiarn

secondou

piwany

Naious

alky

haidey to

ard

ale-koH CH, =cH

depeudi

g

vpon

stabiu

y ot

prdct

alkene

Conidenng

byter

Doujugatton

CH

,echa

Ik

the

Subtrae

conn

o

Man

one

lype

o

Wajpw dot deponc

() cHz-cty- cHcH Br

(u)fo liina Dibides

De

CHg-Ct,-c-cHa

Suyi2elf

YXn

(V) fo Alcohols

ViCinal
Dihalida
(halogeus ave

oo

djalnt

e

alo)on

oat r

alc: koH "

=2b.waor.

Conc

Hocfwawn

t lzucl

de haloanctn.

alcoh s alsu an xme of p enorto in

waloMas ao treatd

Can

bocahón

te

trelet

depemM

Carb cald

-Ve

all nes

CHg- CH

’R -cHa-ce

CEt adt)

Syn adtn

Ni

Yodwctibli

wmley

Hz

n its

bouny

fomt

4hte

CHEMIAC PRopERIEI

Anode

\CH

CHaCHz

Ehene

1s

colourles

j

sWee{ dov'y le

pCH =CH

PHNSICAL PPOPEPTES

\ibereted,at cathode ewe to

HI

Cu-Cu

Ptts uccinate

C-oK

alL

cH

alene

N)

koL

BE'S

ELECI2oSS.

P tasium

ao

di

acidcaiboyieon

electoyir

Cla - cH= CH- CH

Chheretea)

Addition of Halbqons

Addi tho

place

Meh:

Aken

on

addition

h

baogens

undsi

apPopiate

Produce

Widnal

oi

haides

Yeddush

Peagent -

Coxpehnut)

cH

H

CH

t

Br-

Bi

1

pr

oloY

CHz

1

CH- CHy- CHy-ty

1

o( Bwhiine (Bra)

nytas:

cndns

decoloursati

Uwsaturattsn

bvdOMi

yare

non classrco|ct