42-L ODIT- 6

stit
Ctyclca (KanS (qotosnakHns)
Cntant 2

aiclopoopone
poopone
Cucdo butane
ectane
yclopentorE
Denlans
tatoruraE

amothos fosm ong.

Afphoko cyctio Gmpord o ydre clsphato Gmpcerd
aoe nown as Attoyetto oopound.

TwPAC
( rnettuyene Cuycto ogane
Retoa methelerga
Peraorn.eBhalere

Ulhel,12-dimeig

Stbshkictt-¥

Ocus
poss b e
Aumeo.
 Totng Conlans cocrst.nomber of CaroDon abm
tHan Stubs}itient hon WCompcuod s nocu

pachercnce is given b
tereftetfab r_ak
Cobon toms

9 Cycbbutyl hvane

IPaxs

etRep©opHepte-heao

Tno ot Corbon aloms aod to Sde chaio

hon e Sde hatn isSabghluen CansE

IC'menylehl)Cuclopoog

E r t o l r e y 8 : C D E - 2 - o n e
 pap-Feic

Cudopenta ,adiene (aouve

Cuclopenta- 1,3-dtene x
Srtt

Cl,4-Ditateatkane) sholopenefcn

oMOP 8-
ocuTs method9-diehelcgen dertvalrve ryblatkan

copaopane
T3-dbromopoog

Ly-Dboutare yelobulare
troutakonE
open cheD alkane,
3) Sutkable e Oo Porph Gf Only "Coclopoopcme.

n o n e

Coborr
 oto-rimes

) 19) &do addikion otfon

CH2 =Ct
CH Cudo b u t a n e

thene
9 Ores- Aides Tactons
Cdiencamt

(Ut 2)Cycloacdiion
13-Rutadrene

513K
Cyclo honome

18

Tetqt Cocte-testone

5 keduoton ot ch Cosbony Gmpocmd

Cemmet

HCT
CcydoUNaTrorej

L t a telopei ua0

astfal oedteqfon-UHuty/ kn8tta

 -o t

piecmaon (orderalon8

Acipic fasIErr
3-KetoErst63
Jaot Ca0
- ,

HEDpenlaror

CyclopenBane

Koolys' Chvna Ocament tn @sehe of CUpgED)

CPyoolysis ot a Eo alt ot dicabouio a a
CosCcenus Metha
Cod ZnCrq7

cce
Cyctopenmore

PpecEs
yclcalkpne Sernebles fhe Conespomdsn pen
Chaey orvpond. bt thorr M,P, density 8P ode hahe
h a Komes.
 f h s feoo b membans (AU) ae gars e
Cohile olhor are clgeetds. Cdue
to less am dor
cucll Foces).
g hteo ham cunle

elooea

Chemia pperktes CKeac Homs)

DFore adica Substu Hon8
HCI
Chlovodyeloporus
tHOT

Brromocyco bufonë

) Adcifon otacHon
a) halogens CROPAME)

bHocl0genacids

A d of Hycoo@en
 CBUTADE)

HET

-Boo00 butone n-ttane

1,4-Dichooobalane

eaey's Sroaln Maoy

1885 Adolt rBaeye als
poskelales3-
I- In Cycloculkanes Each abon cetom
p hydotd oonded to glflor 4Cobon
oms e amgle
beyD Fy_aiy of adiacen
bond Shcud be Efvaheara Ctoq)
2 Dut to Cyclta matcroe Cyclaalanes CrOe planO
natoe a s a fto bond angle bcth
oTsa
aLolacen raton atom in e onq qe no clomqe
cual to noomal teloa hedoal aqle te 1oqs°,
ho anoke deyiafto) Vanies h Sze ot otn
3- Rny dustdotoo oo deviaton ron
hveo angleQues a Soaln n
the otrg Cm
hslaloility to yestellopf noleccele
This Shratn Knotn as Atgle slos n

Angle Shui 0q. Bond cpqle to plar

 - qot to5 ho dlevrakoo Foom Uoomal arqle tog
wilN be amale soain amd henoe
Occkbvr Of yctoalKorme
6- Move the2 STabiur OF othg ustem t ore
easty foomooo
efFeomarion of GcloalKene docot oehho.ko
Sabiuk dolng
Stability ot
Angle Soatn.

OmpouMq Ingoral Ple sCun

Cobon cefo0s Bond agle|
CytlopoopUe 4(I09-Co): q4|
yclo butane
Colo pentaroe (O8°
Cyclo hoxcrne 20
57
Ceyclohetpland (23.
baxet-q.33
6 Culo ootone 13 12.4

Bond Crdle 180 Cn-a)

1B0 XS Seo
 (OD

pt1s-

vceDces -
HeaF ot Combustione

G86K/mol

smallr ho VQlue cd haa ot Combuston pe Ch 9otup

G53 5K30ol

mtalton
Bayors soaup Could nob plaun e Fomatton of
alkere.
Acordung to Byo S*uD MoOO:6,Y Shocel
oe Tess Sluble
 Chauolans
etipor-5agntd
j smabe

oxuisons mol{s malilicattong. cgclchoreme i moe

Stabre nu CydepenlarE

Ha

Ha

Fta

at voal eQtoota
Cup or doruun socu Ava