1 Ethyl 3 3 Dimethylcyclohexane
a.
The IUPAC proper name is given as 3-ethyl-2-methylhexane.
The given molecule has the longest concatenation of vi carbons (hexane) with methyl and ethyl substituents at the second and third positions.
The structure of the given molecule is shown below:
three-ethyl-2-methylhexane
b.
The IUPAC proper name is given assec-butylcyclopentane.
The given molecule has a cyclic group of six carbons (cyclohexane) with the substituent sec-butyl at the offset position.
The structure of the given molecule is shown beneath:
sec-butylcyclopentane
c.
The IUPAC proper name is given equally 4-isopropyl-2,4,v-trimethylundecane.
The given molecule has a circadian group of 11 carbon chains with the substituent isobutyl at the fourth positionand the methyl groups at the 2nd, fourth, and 5th positions.
The structure of the given molecule is shown below:
four-isopropyl-ii,4,5-trimethylundecane
d.
The IUPAC name is given as cyclobutylcycloheptane.
The given molecule is composed of aseven-carbon cyclic ring with the substituent cyclobutyl at the first position.
The construction of the given molecule is shown beneath:
Cyclobutylcycloheptane
eastward.
The IUPAC name is given every bit 3-ethyl-ane,1-dimethylcyclohexane.
The given molecule comprises a six-carbon cyclic ring with the substituent ethyl at the third position and two methyl atoms at the first position.
The structure of the given molecule is shown below:
3-ethyl-1,1-dimethylcyclohexane
f.
The IUPAC name is given as4-butyl-1,one-diethylcyclooctane.
The given molecule is an eight-carbon circadian ring with the substituent butyl at the fourth and two ethyl groups at the first position, respectively.
The construction of the given molecule is shown below:
4-butyl-1,1-diethylcyclooctane
yard.
The IUPAC name is given as half-dozen-isopropyl-2,3-dimethyldodecane.
The given molecule comprises a 12-carbon chain with the substituents isopropyl at the sixth position and two methyls at the 2d and third positions.
The construction of the given molecule is shown below:
half dozen-isopropyl-2,3-dimethyldodecane
h.
The IUPAC proper noun is given as ii,two,6,6,7-pentamethyloctane.
The given molecule is composed ofeight carbon chains with methyl substituting at the second, 6th, and seventh positions.
The structure of the given molecule is shown below:
2,2,6,6,7-pentamethyloctane
i.
The IUPAC name is given ascis-i-ethyl-3-methylcyclopentane.
The given molecule comprises a five-carbon cyclic ring with methyl substituting at the third and ethyl at the fifth positions. Both substituents are on the same side of the band.
The structure of the given molecule is shown below:
cis-i-ethyl-3-methylcyclopentane j. The IUPAC name is given as trans-1-tert-butyl-four-ethylcyclohexane.
The given molecule comprises 6 carbon atoms in a cyclic ring with the substituents ethyl at the fourth and tert-butyl at the first positions. Both substituents are on the contrary side of the ring.
The structure of the given molecule is shown below:
trans-1-tert-butyl-4-ethylcyclohexane
1 Ethyl 3 3 Dimethylcyclohexane,
Source: https://www.studysmarter.us/textbooks/chemistry/organic-chemistry-5th/alkanes/q40-question-draw-the-structure-corresponding-to-each-iupac-/
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