Hyperconjugation
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The order of heat of hydrogenation in following compound is:
- I < II < IV < III
- III < IV < II < I
- II < III < I < IV
- II < IV < I < III
- CH≡CH>CH2=CH2>CH3−C≡CH>CH3−CH3
- CH3−CH3>CH2=CH2>CH3−C≡CH>CH≡CH
- CH2=CH2>CH3−CH=CH2>CH3−C≡CH>CH≡CH
- CH≡CH>CH3−C≡CH>CH2=CH2>CH3−CH3
Consider the following compounds
hyperconjugation occurs in
I only
II only
I and III
III only
- (CH3)2HC+
- H3C+
- CH3CH+2
- (CH3)3C+
- II>III>I
- I>II>III
- II>I>III
- I>III>II
Why hyperconjugation is called no bond resonance?
And how synergic effect strengthens the bond between metal and the carbonyl group ??????
- A carbanion (−−CH2)
- A free radical (−∙CH2)
- A carbocation (−+CH2)
- A double bond >C=C<
Which of The Following Molecule Is Planar?
- It is a destabilizing effect.
- Takes place when α-hydrogens are there in a conjugated system.
- The electron density flows from σ-orbital to empty p-orbital.
- Ph−CCl3 shows +H effect (hyperconjugation) due to presence of α-chlorines.
Write the two chemical tests to distinguish ethyne and ethene
But I am not able to calculate it using the formula 1/2[V+L+A-C] . Can I please get help?
How can I distinguish the functional group region and fingerprint region in an infrared spectrum?
CH3−CH=CH2(I)
CH3−C|CH3=C|CH3−CH3(II)
CH3−C|CH3=CH2(III)
CH3−C|CH3=CH−CH3(IV)
- I < III < IV < II
- I < II < III < IV
- IV < III < II < I
- II < III < IV < I
- (I)>(II)>(IV)>(III)
- (I)>(III)>(IV)>(II)
- (II)>(III)>(IV)>(I)
- (IV)>(II)>(I)>(III)
Heat of hydrogenation of cyclohexane is -119KJ and heat of hydrogenation of benzene is 206KJ/mole. Find the resonance energy of benzene.
Why there is no Hyperconjugation in Carbanion?
The arrangement of (CH3)3C−, (CH3)2CH− , CH3CH2− when attached to a benzene or an unsaturated group in increasing order of inductive effect effect is.
The correct order of stability for the following alkoxides is:
(C) > (A) > (B)
(C) > (B) > (A)
(B) > (A) > (C)
(B) > (C) > (A)
Give the condition for hyperconjugation?
Which of the following alkyl group has the maximum hyperconjugation effect and least +I effect?
(CH3)2CH
CH3CH2 -
CH3-
(CH3)3C-
- I>II>III
- I>III>II
- III>II>I
- II>III>I
In which of the following carbocation, there is maximum stabilization due to the hyperconjugation effect?
Neopentyl
Tert-Butyl
Isopropyl
Ethyl
Explain why alkyl groups act as electron donors when attached to a π system.
The stability of (CH3)2C=CH2 is more than that of CH3CH2CH=CH2 due to
inductive effect of the methyl group
resonance effect of methyl group
hyperconjugative effect of the methyl group
resonance and inductive effect of methyl group.