13. Ethylethanoate and butanoic acid can be classified as A. positional isomers B. chain isomers C. functional isomers D. stereoisomers

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13. Ethylethanoate and butanoic acid can be classified as
A. positional isomers
B. chain isomers
C. functional isomers
D. stereoisomers
14. Which of the following pairs are positional isomers
A. trans-1,4-dichlorocyclohexane, cis-1,3-dichlorocyclopentane
B. trans 1,4-dichlorocyclohexane, cis-1,4-dichlorocyclohexane
C. 2-pentanol, Cyclopentanol
D. 1,2-cycohexanediol, 1,3-cycohexanediol
15. Which of the following compounds will have zero dipole moment?
A. cis-1,2-dibromoethylene
B. 1,1-dibromoethylene
C. trans-1,2-dibromoethylene
D. all of these
16. Which of the following is not aromatic:
A. cyclopentadienyl cation
B. cyclopentadienyl anion
C. Cyclopropenyl cation
D. Cycloheptatrienyl cation
17. Which of the following compounds containing lone pair has the least
tendency to donate its electrons?
A. the lone pair in pyridine
B. the lone pair in furan
C. the lone pair in pyrole
D. the lone pair in thiophene
Transcribed Image Text:13. Ethylethanoate and butanoic acid can be classified as A. positional isomers B. chain isomers C. functional isomers D. stereoisomers 14. Which of the following pairs are positional isomers A. trans-1,4-dichlorocyclohexane, cis-1,3-dichlorocyclopentane B. trans 1,4-dichlorocyclohexane, cis-1,4-dichlorocyclohexane C. 2-pentanol, Cyclopentanol D. 1,2-cycohexanediol, 1,3-cycohexanediol 15. Which of the following compounds will have zero dipole moment? A. cis-1,2-dibromoethylene B. 1,1-dibromoethylene C. trans-1,2-dibromoethylene D. all of these 16. Which of the following is not aromatic: A. cyclopentadienyl cation B. cyclopentadienyl anion C. Cyclopropenyl cation D. Cycloheptatrienyl cation 17. Which of the following compounds containing lone pair has the least tendency to donate its electrons? A. the lone pair in pyridine B. the lone pair in furan C. the lone pair in pyrole D. the lone pair in thiophene
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