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Point out the incorrect statement about resonance?
The resonating structures should have same number of electron pairs.
Which of the following ions is the most resonance stabilised?
Phenoxide ion shows maximum resonating structures.
Hyperconjugation is
Hyperconjugation involves conjugation of a electrons of C - H bond and π electrons of multiple bond.It is noticed due to delocalisation of σ- and π-bonds. It is . also known as no bond resonance.
The number of hyperconjugating structures shown by the carbocations are given below. Which one is not correctly matched?
shows 6 hyperconjuigatihg structures
In which of the following species hyperconjugation is possible?
For hyperconjugation α-carbon with respect to sp2 hybridised carbon should have at least one hydrogen.
Answer the following question based on the given paragraph.Stability of carbocation, alkylfree radical and alkene can be explained on the basis of hyperconjugation.In all these cases, there is presence ofhydrogen atom at theadjacent carbon atom ofsp2 hybridised carbon atom. Total number of hyperconjugating structures depends upon the number of hydrogen atoms present at adjacent carbon atom of sp2 C-atom.More the hyperconjugating structures, more is the stabihty of the ion.
Decreasingorder of stabilityof following alkenes is(i) CH3 - CH = CH2(ii) CH3 - CH = CH - CH3(iii) (iv)
Which of the following alcohols on dehydration gives most stable carbocation?
Tertiary carbocation is more stable than secondary and primary carbocatioris.
Which of the following contains three pairs of electrons in valence shell?
In carbocations, the carbon atom with positive charge has only 6 electrons in its valence shell.
Stability of alkyl carbocations can be explained by
Stability of alkyl carbocations can be explained by both inductive effect and hyperconjugation.
In the given reaction two products are expected.The product (B) is formed as a major product because
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