Q 1 :    

Which among the following aldehydes is most reactive towards nucleophilic addition reactions?                  [2024]

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(2)

Reactivity of aldehydes and ketones is more in nucleophilic addition reactions if:

(i) Partial positive charge on carbonyl carbon is more, Nu- is attracted more and hence more is reactivity.

(ii) Lesser is crowding around carbonyl carbon, easier is it for Nu- to approach, hence more is reactivity.

Presence of alkyl groups around carbonyl carbon decreases partial positive charge of the carbonyl carbon due to +I effect of alkyl groups. Also, bulky alkyl groups hinder attack of Nu- on carbonyl carbon. Hence presence of alkyl groups around carbonyl carbon decreases reactivity of aldehydes/ketones towards nucleophilic addition.

 



Q 2 :    

The compound formed by the reaction of ethanal with semicarbazide contains ______ number of nitrogen atoms.           [2024]



(3)

 



Q 3 :    

Residue (A) + HCl (dil) → Compound (B)

Structure of residue (A) and compound (B) formed respectively is:     [2025]

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(4)

 



Q 4 :    

Given below are two statements:                [2025]

Consider the following reaction

In the light of the above statements, choose the correct answer from the options given below:

  • Both Statement I and Statement II are false

     

  • Both Statement I and Statement II are true

     

  • Statement I is true but Statement II is false

     

  • Statement I is false but Statement II is true

     

(2)

Lesser is steric hindrance around C=O and more is partial positive charge on the carbon of C=O, easier is the attack by nucleophile.

 



Q 5 :    

Which of the following arrangements with respect to their reactivity in nucleophilic addition reaction is correct?    [2025]

  • p-nitrobenzaldehyde < benzaldehyde < p-tolualdehyde < acetophenone

     

  • acetophenone < p-tolualdehyde < benzaldehyde < p-nitrobenzaldehyde

     

  • benzaldehyde < acetophenone < p-nitrobenzaldehyde < p-tolualdehyde

     

  • acetophenone < benzaldehyde < p-tolualdehyde < p-nitrobenzaldehyde

     

(2)

Lesser is crowding around C=O and more is partial positive charge on carbon of C=O, more is reactivity of carbonyl compounds towards nucleophilic addition. Electron withdrawing groups increase partial positive charge and electron releasing groups decrease partial positive charge on C=O.