Important Questions of Organic Chemistry – Some Basic Principles and Techniques Chemistry | Zigya

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 Multiple Choice QuestionsLong Answer Type

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211.

Write resonance structures of CH= CH–CHO, indicate relative stability of the contributing structures.

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 Multiple Choice QuestionsShort Answer Type

212.

Give reasons why the following two structures I and II cannot be the major contributors to the real structure of CH3COOCH3:



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 Multiple Choice QuestionsLong Answer Type

213.

Explain hyperconjugation effect or no-bond resonance.

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 Multiple Choice QuestionsShort Answer Type

214.

Explain why alkyl groups act as electron donors when attached to a straight pi semicolon minus system.

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 Multiple Choice QuestionsLong Answer Type

215.

What are carbocations? Discuss the relative stabilities of primary, secondary and tertiary carbocations.

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 Multiple Choice QuestionsShort Answer Type

216.

Give two methods for the generation of carbocation. Describe its structure. 

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 Multiple Choice QuestionsLong Answer Type

217.

What are carbanions? How are these generated? Discuss the relative stabilities of primary, secondary and tertiary carbanions.

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 Multiple Choice QuestionsShort Answer Type

218.

Why carbanions are very negative? Discuss the structure of carbanion.

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 Multiple Choice QuestionsLong Answer Type

219.

What are free radicals? How are these formed? Discuss the structure of free radicals.

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220. With the help of hyperconjugation effect, explain which of the following free radicals is the most stable:

bold C with bold asterisk times on top bold H subscript bold 3 bold space bold comma bold space bold left parenthesis bold CH subscript bold 3 bold right parenthesis subscript bold 2 bold C with bold asterisk times on top bold H bold space bold comma bold CH subscript bold 3 bold C with bold asterisk times on top bold H subscript bold 2 bold comma bold C with bold asterisk times on top bold left parenthesis bold CH subscript bold 3 bold right parenthesis subscript bold 3
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