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Nomenclature of Cyclo Compounds
Nomenclature of Cyclo Compounds
yl or orginq all'eyoli
The ame8 op alcyC Coopouros ae Obtan
to Hhe
yclo
odd
hame OP
e re x
Commeapod
raigh Chos
re)
yorochoin (oikanr, oikeng
) i
Ch CHa Cyelobu)ane
lope arr
Cyolopropone
aphabeical Orde r
he owgs}
loca prrovided+ dos ot
Pe nt Cyolopentane
CH2-CH,:(HN
9-Cyolopropye prop- ne
C4= H - CH
3
icyolic reng
ban
o a nql ohan
CtHacrd
homed 3qerivative
COropound
sp«cives
O)kanc
Carbon Ctom
Chain
- CH2
Dicyclopropylmeane
) 3
1,3dicycohexypro
mol4ple bon and8ome oth
are prosent
substituenjs
The Doberung ore
he Careba qdo
ceay ha
uHiple bond ge opst lacant
7uO Ond
an bsti+uent er 9ro
One
an
ooan a t he Pira
e acoeT
poi oF inneronoe.
2
3- Aln oCyclo heper
cyolopenione
-CH3
1, 5-methyecyoio hex 1- ene
ol
-(Cyclopent on 4 ) Propon
CH 2
CH H - CooH
)
Opal CH C 1 -COoH
OH
CHa-CH*CH AH -CHa
1
2
h/orA
Caycla
3-4ro reethyl
-
2 -
hydroxypy)
cyolohenye benzere)
SO2
H3
CH
3- Methy oyolohexan - o l
2
Dehyt yclohex- 2-enl-cne
cH3
he C-adom OP e
noMe oP hee
notinolude q e ponet
alicyoc 38*em r'
c yC
e ioxane Corbonijele
CHO
beAonccarbod des
Oxoc yclo