+I Effect
Trending Questions
(i) Phenol
(ii) methyl phenol
(iii) meta-nitrophenol
(iv) para-nitrophenol
The acidity order is:
- (iv)>(iii)>(i)>(ii)
- (iii)>(iv)>(i)>(ii)
- (i)>(iv)>(iii)>(ii)
- (ii)>(i)>(iii)>(iv)
- D<A<C<B
- B<C<D<A
- C<B<A<D
- B<C<A<D
The correct order of stability of the following carbanions is:
(CH3)3C−, −CCl3, (CH3)2CH−, C6H5−CH−2
C6H5−CH−2>−CCl3>(CH3)2CH−>(CH3)3C−
None of the above
−CCl3>C6H5−CH−2>(CH3)2CH−>(CH3)3C−
C6H5−CH−2>−CCl3>(CH3)3C−>(CH3)2CH−
- (CH3)3N > (CH3)2NH > CH3NH2
- (CH3)3N > CH3NH2 > (CH3)2NH
- (CH3)2NH > CH3NH2 > (CH3)3N
- (CH3)2NH > (CH3)3N > (CH3)NH2
- I > II > III
- III > II > I
- I > III > II
- II > I > III
Which one is most reactive towards nucleophilic addition reaction?
Alkyl group are o, p - directing because of
Inductive effect
Electromeric effect
Hyperconjugation effect
All the three
Which of the two: O2NCH2CH2O– or CH3CH2O– is expected to be more stable and why?
Species in which hyperconjugation does not occur is
- b>c>d>a
- c>b>a>d
- b>a>c>d
- c>b>d>a
Arrange in the order of increasing acidic strengths.
X > Z > Y
Z < X > Y
X > Y > Z
Z > X > Y
- Phenol is more acidic than benzoic acid
- 4-Chlorophenol is more acidic than phenol
- 4-methylbenzoic acid is less acidic than benzoic acid
- Phenol is less acidic than benzoic acid
- m−NO2−C6H4NH2
- C6H5NH2
- p−NO2−C6H4NH2
- C6H5CH2NH2
- (I) > (II) > (III) > (IV)
- (IV) > (III) > (II) > (I)
- (III) > (IV) > (II) > (I)
- (I) > (II) > (IV) > (III)
- Nucleophilic addition
- Nucleophilic substitution
- Electrophilic substitution
- Electrophilic addition
- −CH3<−H<−D<−T
- −CH3<−H<−T<−D
- −H<−CH3<−T<−D
- −H<−D<−T<−CH3
Which one of the following orders is correct regarding the inductive effect of the substituents?
-NR2<-OR>-F
-NR2>-OR>-F
-NR2<-OR<-F
-NR2>-OR<-F
- −CH−2
- −O−
- All the three groups show similar +I effect.
- −NH−
Major product P is
[0.77 Mark]
1∘Alkyl Group, 2∘Alkyl Group, 3∘Alkyl Groupand Methyl Group
- 1∘Alkyl Group <2∘Alkyl Group <3∘Alkyl Group <Methyl Group
- Methyl Group<1∘Alkyl Group <2∘Alkyl Group <3∘Alkyl Group
- 1∘Alkyl Group <3∘Alkyl Group <2∘Alkyl Group <Methyl Group
- Methyl Group<3∘Alkyl Group <1∘Alkyl Group <1∘Alkyl Group
i. m-nitrophenol ii. m-cresol
iii. phenol .iv m-chlorophenol
- iii < ii < i < iv
- ii < iv < iii < i
- ii < iii < iv < i
- ii < iii < i < iv
- I>III>II>IV
- I>III>IV>II
- II>IV>III>I
- I>II>IV>III
Which of the following will be most acidic?
CH3−COOH
CH3−CH2−COOH
CH3−CH2−CH2−COOH
CH3−CH2−CH2−CH2−COOH
- −CN
- −NH−
- −CH−2
- −CH3
What is meant by the term average bond enthalpy? Why is there difference in bond enthalpy of O−H bond in ethanol (C2H5OH) and water?
I. CH3−CH2−CD+2
II. CH3−CH2−CT+2
(Explain on the basis of inductive effect)
- I is more stable than II
- II is more stable than I
- Both are equally stable
- Stability criterion cannot be applied in this case
- −CH3
- −CH2−CH3
- −C(CH3)3
- All of the above.