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Teacher in-charge: Pradnya.G.Gondane
Presented by: Khushbu Sharma
M.Pharm. I year
P.G Department of Pharmaceutical Chemistry
Gurunanak College of Pharmacy, Nagpur
1.Stability of free radicals can be
explained on the basis of ______.
a) Inductive effect.
b) Electromeric effect.
c) Hyperconjugation.
d) Mesomeric effect.
Ans: C
Clarification: Stability of free radical can be
explained on the basis of hyperconjugation
effect and ease of formation.
2.The hybridisation of carbocation is
_______ .
a)Sp
b)Sp2
c)Sp3
d)Sp3d
Ans:b
Clarification: The hybridisation of
carbocation is Sp2. A carbocation is
molecule in which a carbon atom bears
and a positive charge.
3.Arrange the following carbocations
in the order of increasing stability.
a)Benzyl> 30 >20 >10
b)Benzyl> 10 >20 >30
c)30 > 20 > 10 >Benzyl
d)10 >20 >30 > Benzyl
Ans: a
Clarification: Benzyl carbocation is the most
stable and 10 carbocation is least stable.
4.The shape of carbotion is ________ .
a)Pyramidal
b)Bent
c)Linear
d)Trigonal planar
Ans: d
Clarification: The shape of the carbocation
is a trigonal planar. It is sp2 hybridised. A
carbocation is molecule in which a carbon
atom bears three bonds and a positive
charge.
5.Carbonium ions are the intermediates in which
the positive charge is carried by the carbon atom
with _____ electrons in the valence shell.
a)6
b)5
c)4
d)3
Ans: a
Clarification: Carbonium ions are the
intermediates in which the positive charge is
carried by the carbon atom with six electrons in
the valence shell. It is an organic cation in which
the positive charge is located on a carbon atom.
6.Positive charge of carbocations can be
dispersed by______ .
a)(+I) effect of alkyl group
b)Resonance in allyl or benzyl carbocation
c)Hyperconjugation in 10 , 20 , 30
carbotions
d)All of the mentioned
Ans: d
Clarification: Positive charge of carbocations can
be dispersed by (+I) effect of the alkyl group or
by resonance in allyl or benzyl carbocation or by
hyperconjugation in 10 ,20 ,30 carbocations.
7.Alkyl substitution at the carbon
bearing positive charge
stabilizes carbocations.
a) True
b)False
Ans: a
Clarification: Alkyl substitution at the carbon
bearing positive charge stabilizes carbocartions.
Carbocation is a molecule in which a carbon
atom bears three bonds and a positive charge.
8.The formal charge at the
carbocaton is equals to _____ .
a) -1
b) 0
c) +1
d) +2
Ans: c
Clarification: A carbocation is molecule in
which a carbon atom bears three bonds and
a positive charge.
9,. The homolytic bond dissociation
energy is inversely proportional to the
______.
a)Bond length
b)Ease of formation
c)Dipole moment
d)All of the mentioned
Ans: b
Clarification: The homolytic bond dissociation
energy is inversely proportional to the ease
of formation of free radicals. Free radicals do
not carry any charge.
10. Which of the following free radical
has the maximum ease of formation?
a)10
b)20
c)30
d)CH3
Ans: c
Clarification: 30 free radical has the maximum
ease of formation. Free radicals do not carry
any charge.
11.Which carbocation is the most
stable?
Ans: b
Clarification: This is stabilized by extended
conjugation. The more adjacent methyl groups
are there, the larger hyperconjugation
stabilization is because of the increased number
of the adjacent C-H bonds.
12.Which one among the following
carbocations has the longest half-
life?
Ans: a
Clarification: Higher the stability of the cation
more will be its half-life. As, in the carbocation, p
orbital overlap with the compound, with the
compound, will be more stabilizing factor then
aromaticity.
13.The order of decreasing stability of the
following cation is?
I)CH3 C+ HCH3 (II) CH3 C+ HOHCH3 (III)CH3
C+ HCOCH3
a)III> II> I
b)I> II>III
c)II> I> III
d)I> III> II
Ans: a
Clarification:At a) , mesomeric effect stabilizes
the carbocation , so its highly stabilized.
14. Which if the following is most
stable intermediate?
Ans: c
Clarification: Stabilized by +M effect of OH
and hyperconjugaton effect .
15.Which intermediate is involved in the
reaction given below ?
a)free radical
b)carbocation
c)carbanion
d)carbene
Ans:d
Clarification: As we can see, in
the first step in the presence to
the light carbene is formed.
16.Amongs the following which is the
most stabilized cation?
Ans: c
Clarification: The positive charge of the
carbon will be stabilised by mesomeric effect
of –NH2 group.
17.Arrange the following intermediate
into decreasing order of stability.
a)I> II>III> IV
b)II> IV >III >I
c)II> I> IV >III
d)II> I >III >IV
Ans:d
Clarification: Mesomeric effect will
stabilize carbocation is highly stable.
+M effect of –NH2 > -OH
18.Arrange the following intermediate into
decreasing order of stability.
a)I> III> II> IV
b)II> III> IV> I
c)III> IV> II> I
d)I> III> IV> II
Ans: a
Clarification: Mesomeric effect will
stabilize carbocation is highly stable.
19.What is the correct decreasing
order of stability of following cation?
a) II>III>I>IV
b) IV> II>III>I
c) IV>III>I>II
d) III>I>II>IV
Ans:b
Clarification: I)it is destabilised by –M and high
–I effect
20.What is the correct decreasing order of
stability of the following cation?
a)I>II>III>IV
b)I>IV>II>III
c)I>III>II>IV
d)IV>III>II>I
Ans:c
Clarification: High +I, therefore the
stability order I>III>II>IV.
Mcqs on carbocations

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Mcqs on carbocations

  • 1. Teacher in-charge: Pradnya.G.Gondane Presented by: Khushbu Sharma M.Pharm. I year P.G Department of Pharmaceutical Chemistry Gurunanak College of Pharmacy, Nagpur
  • 2. 1.Stability of free radicals can be explained on the basis of ______. a) Inductive effect. b) Electromeric effect. c) Hyperconjugation. d) Mesomeric effect. Ans: C Clarification: Stability of free radical can be explained on the basis of hyperconjugation effect and ease of formation.
  • 3. 2.The hybridisation of carbocation is _______ . a)Sp b)Sp2 c)Sp3 d)Sp3d Ans:b Clarification: The hybridisation of carbocation is Sp2. A carbocation is molecule in which a carbon atom bears and a positive charge.
  • 4. 3.Arrange the following carbocations in the order of increasing stability. a)Benzyl> 30 >20 >10 b)Benzyl> 10 >20 >30 c)30 > 20 > 10 >Benzyl d)10 >20 >30 > Benzyl Ans: a Clarification: Benzyl carbocation is the most stable and 10 carbocation is least stable.
  • 5. 4.The shape of carbotion is ________ . a)Pyramidal b)Bent c)Linear d)Trigonal planar Ans: d Clarification: The shape of the carbocation is a trigonal planar. It is sp2 hybridised. A carbocation is molecule in which a carbon atom bears three bonds and a positive charge.
  • 6. 5.Carbonium ions are the intermediates in which the positive charge is carried by the carbon atom with _____ electrons in the valence shell. a)6 b)5 c)4 d)3 Ans: a Clarification: Carbonium ions are the intermediates in which the positive charge is carried by the carbon atom with six electrons in the valence shell. It is an organic cation in which the positive charge is located on a carbon atom.
  • 7. 6.Positive charge of carbocations can be dispersed by______ . a)(+I) effect of alkyl group b)Resonance in allyl or benzyl carbocation c)Hyperconjugation in 10 , 20 , 30 carbotions d)All of the mentioned Ans: d Clarification: Positive charge of carbocations can be dispersed by (+I) effect of the alkyl group or by resonance in allyl or benzyl carbocation or by hyperconjugation in 10 ,20 ,30 carbocations.
  • 8. 7.Alkyl substitution at the carbon bearing positive charge stabilizes carbocations. a) True b)False Ans: a Clarification: Alkyl substitution at the carbon bearing positive charge stabilizes carbocartions. Carbocation is a molecule in which a carbon atom bears three bonds and a positive charge.
  • 9. 8.The formal charge at the carbocaton is equals to _____ . a) -1 b) 0 c) +1 d) +2 Ans: c Clarification: A carbocation is molecule in which a carbon atom bears three bonds and a positive charge.
  • 10. 9,. The homolytic bond dissociation energy is inversely proportional to the ______. a)Bond length b)Ease of formation c)Dipole moment d)All of the mentioned Ans: b Clarification: The homolytic bond dissociation energy is inversely proportional to the ease of formation of free radicals. Free radicals do not carry any charge.
  • 11. 10. Which of the following free radical has the maximum ease of formation? a)10 b)20 c)30 d)CH3 Ans: c Clarification: 30 free radical has the maximum ease of formation. Free radicals do not carry any charge.
  • 12. 11.Which carbocation is the most stable? Ans: b Clarification: This is stabilized by extended conjugation. The more adjacent methyl groups are there, the larger hyperconjugation stabilization is because of the increased number of the adjacent C-H bonds.
  • 13. 12.Which one among the following carbocations has the longest half- life? Ans: a Clarification: Higher the stability of the cation more will be its half-life. As, in the carbocation, p orbital overlap with the compound, with the compound, will be more stabilizing factor then aromaticity.
  • 14. 13.The order of decreasing stability of the following cation is? I)CH3 C+ HCH3 (II) CH3 C+ HOHCH3 (III)CH3 C+ HCOCH3 a)III> II> I b)I> II>III c)II> I> III d)I> III> II Ans: a Clarification:At a) , mesomeric effect stabilizes the carbocation , so its highly stabilized.
  • 15.
  • 16. 14. Which if the following is most stable intermediate? Ans: c Clarification: Stabilized by +M effect of OH and hyperconjugaton effect .
  • 17. 15.Which intermediate is involved in the reaction given below ? a)free radical b)carbocation c)carbanion d)carbene Ans:d
  • 18. Clarification: As we can see, in the first step in the presence to the light carbene is formed.
  • 19. 16.Amongs the following which is the most stabilized cation? Ans: c Clarification: The positive charge of the carbon will be stabilised by mesomeric effect of –NH2 group.
  • 20. 17.Arrange the following intermediate into decreasing order of stability. a)I> II>III> IV b)II> IV >III >I c)II> I> IV >III d)II> I >III >IV
  • 21. Ans:d Clarification: Mesomeric effect will stabilize carbocation is highly stable. +M effect of –NH2 > -OH
  • 22. 18.Arrange the following intermediate into decreasing order of stability. a)I> III> II> IV b)II> III> IV> I c)III> IV> II> I d)I> III> IV> II
  • 23. Ans: a Clarification: Mesomeric effect will stabilize carbocation is highly stable.
  • 24. 19.What is the correct decreasing order of stability of following cation? a) II>III>I>IV b) IV> II>III>I c) IV>III>I>II d) III>I>II>IV
  • 25. Ans:b Clarification: I)it is destabilised by –M and high –I effect
  • 26. 20.What is the correct decreasing order of stability of the following cation? a)I>II>III>IV b)I>IV>II>III c)I>III>II>IV d)IV>III>II>I
  • 27. Ans:c Clarification: High +I, therefore the stability order I>III>II>IV.