Home
Class 12
CHEMISTRY
Most reactive towards nucleophilic addit...

Most reactive towards nucleophilic addition is

A

p-tolualdehyde

B

4-nitrobenzaldehyde

C

benzaldehyde

D

acetophenone

Text Solution

Verified by Experts

The correct Answer is:
B
Doubtnut Promotions Banner Mobile Dark
|

Topper's Solved these Questions

  • ALDEHYDES AND KETONES

    AAKASH SERIES|Exercise objective Exercise -61|1 Videos
  • ALDEHYDES AND KETONES

    AAKASH SERIES|Exercise objective Exercise -62|1 Videos
  • ALDEHYDES AND KETONES

    AAKASH SERIES|Exercise objective Exercise -59|1 Videos
  • ALCOHOLS, PHENOLS AND ETHERS

    AAKASH SERIES|Exercise ETHERS (OBJECTIVE EXERCISE-4)|50 Videos
  • ALKYL AND ARYL HALIDES

    AAKASH SERIES|Exercise OBJECTIVE EXERCISE - 4 (ASSERTION (A) & REASON (R) TYPE QUESTIONS)|19 Videos

Similar Questions

Explore conceptually related problems

Aldehydes and ketons are susceptible to nuclephlic addition because carbonylgroup Polar (due to electronegativeity difference between carbon and oxygen positive charge on carbonyl compound towards nucleophilic . this addition is catalysed by acid . REactivity of carbonyl compound towards nuclephilic addotion increase with increase in teh electron deficiency at carbonyl carbon Thus (-I.E ) groups increase while (+I.E ) groups decreases the reactivity of carbonyl compound . which among the following isomeric compound is most reactive towards nucleophilic addition

Ethanal is more reactive towards nucleophilic addition reaction than propanone. Why ?

Knowledge Check

  • The following is more reactive towards nucleophilic addition reactions

    A
    `CH_3 COCH_3`
    B
    `HCHO`
    C
    `CH_3 CHO`
    D
    `C_2 H_5CHO`
  • Which of the following is least reactive towards electrophilic addition ?

    A
    B
    C
    D
  • Which of the following is least reactive towards electrophillic addition

    A
    B
    C
    D
  • Similar Questions

    Explore conceptually related problems

    Aldehydes and ketons are susceptible to nuclephlic addition because carbonylgroup Polar (due to electronegativeity difference between carbon and oxygen positive charge on carbonyl compound towards nucleophilic . this addition is catalysed by acid . REactivity of carbonyl compound towards nuclephilic addotion increase with increase in teh electron deficiency at carbonyl carbon Thus (-I.E ) groups increase while (+I.E ) groups decreases the reactivity of carbonyl compound . which among the following is most reactive towards nuclephilic addition

    Arrange the following in increasing order of reactivity towards nucleophilic addition. HCHO , CH_(3)CHO and CH_(3)COCH_(3)

    Which carbonyl group of the given compound in most reactive for nucleophilic addition reaction ?

    Which of the following is the most reactive towards nucleophilic substitution by NaOH

    Which of the following is least reactive towards nucleophilic substitution with aqueous KOH?