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Aldehyde and ketones are specially susce...

Aldehyde and ketones are specially susceptible susceptible to nucleophile addition because carbonyl group (due to electronegatvity different between carbon and oxygen).

Positive charge on carbon makes it reactive towards the nucleophile. This addition is catalysed by acid. Reactivity of carbonyl compound towards nucleophilic addition increases in the electron deficience at carbonyl carbon. Thus, (-I.E.) group increase while (+I.E.) groups decrease the reactivity of carbonyl compound
Carbonyl compounds show nucleophilic addition with:

A

HCN

B

`NaHSO_(3)`

C

`(CH_(3)OH+HCl)`

D

all of these

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The correct Answer is:
D
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Aldehyde and ketones are specially susceptible susceptible to nucleophile addition because carbonyl group (due to electronegatvity different between carbon and oxygen). Positive charge on carbon makes it reactive towards the nucleophile. This addition is catalysed by acid. Reactivity of carbonyl compound towards nucleophilic addition increases in the electron deficience at carbonyl carbon. Thus, (-I.E.) group increase while (+I.E.) groups decrease the reactivity of carbonyl compound Select the least reactive carbonyl compound for nucleophilic addition:

Aldehyde and ketones are specially susceptible susceptible to nucleophile addition because carbonyl group (due to electronegatvity different between carbon and oxygen). Positive charge on carbon makes it reactive towards the nucleophile. This addition is catalysed by acid. Reactivity of carbonyl compound towards nucleophilic addition increases in the electron deficience at carbonyl carbon. Thus, (-I.E.) group increase while (+I.E.) groups decrease the reactivity of carbonyl compound Which among the following carbonyl compounds is most polar?

Aldehyde and ketones are specially susceptible susceptible to nucleophile addition because carbonyl group (due to electronegatvity different between carbon and oxygen). Positive charge on carbon makes it reactive towards the nucleophile. This addition is catalysed by acid. Reactivity of carbonyl compound towards nucleophilic addition increases in the electron deficience at carbonyl carbon. Thus, (-I.E.) group increase while (+I.E.) groups decrease the reactivity of carbonyl compound Which of the following is most reactve to give nucleophilic addition?

The reactivity of carbonyl compounds towards nucleophilic addition reaction gets affected by

The order of reactivity of carbonyl compounds for nucleophilic addition is

Carbonyl compounds undergo nucleophilic addition because of :

Discuss the relative reactivities of carbonyl compounds in nucleophilic addition reactions.

The relative reactivities of acyl compound towards nucleophilic substitution are in the order of

Which one is most reactive towards nucleophilic addition reaction?

What is the order of reactivity of the following compounds towards nucleophilic substitution?

ALLEN-ALKENE, ALKANE & ALKYNE -EXERCISE-3
  1. Aldehydes and ketones are amphoteric. Thus they can act both as acids ...

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  2. Aldehydes and ketones are amphoteric. Thus they can act both as acids ...

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  3. Aldehydes and ketones are amphoteric. Thus they can act both as acids ...

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  4. Aldehyde and ketones are specially susceptible susceptible to nucleoph...

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  5. Aldehyde and ketones are specially susceptible susceptible to nucleoph...

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  6. Aldehyde and ketones are specially susceptible susceptible to nucleoph...

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  7. Aldehyde and ketones are specially susceptible susceptible to nucleoph...

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  8. Aldehyde and ketones are specially susceptible susceptible to nucleoph...

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  9. The origin of acidity and basicity in organic compound is great intere...

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  10. The origin of acidity and basicity in organic compound is great intere...

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  11. The origin of acidity and basicity in organic compound is great intere...

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  12. The origin of acidity and basicity in organic compound is great intere...

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  13. The origin of acidity and basicity in organic compound is great intere...

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  14. Diazonium salt formation and coupling reaction: When a reaction mixtur...

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  15. Diazonium salt formation and coupling reaction: When a reaction mixtur...

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  16. Diazonium salt formation and coupling reaction: When a reaction mixtur...

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  17. Amines are derivatives of ammonia and are classified as 1^@, 2^@ , and...

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  18. Amines are derivatives of ammonia and are classified as 1^(@), 2^(@), ...

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  19. Amines are derivatives of ammonia and are classified as 1^@, 2^@ , and...

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  20. Amines are derivatives of ammonia and are classified as 1^@, 2^@ , and...

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