CameraIcon

SearchIcon

MyQuestionIcon

1

You visited us 1 times! Enjoying our articles? Unlock Full Access!

Formation of Diazonium Salts

Select the in...

Question

Select the incorrect option for the following statements. (a) bimolecular elimination of alkyl halides is a stereo specific reaction (b) inner SN2 reaction a single isomer is the only product (c) n-propyl alcohol dehydrates in strongly basic conditions by E1cB mechanism (d) 3-hydroxypropanal dehydrates in strongly basic conditions by E1cB mechanism

Open in App

Solution

Suggest Corrections

thumbs-up

1

Similar questions

Q. An incorrect statement with respect to

S_{N} 1

S_{N} 2

mechanism for alkyl halide is :

Q. Alkyl halides and alcohols easily undergo nucleophilic substitution either through

S_{N} 1

S_{N} 2

mechanism. The relative case of these two processes depends upon the nature of the substrate (alkyl group) as well as leaving group, nature of nucleophile and also upon the nature of the solvent.

S_{N} 1

mechanism involves the formation of carbocation as intermediate while

S_{N} 2

mechanism involves the formation of a transition pentavalent state.

S_{N} 1

is the main mechanism in

3^{0}

alkyl halides and alcohols, while

S_{N} 2

mechanism is the path adopted by most of the

1^{o}

2^{o}

alkyl halides may follow

S_{N} 1

S_{N} 2

.

What happens when

1^{o} R O H

H X

Q. Which of the following alkyl halide is most reactive towards substitution on reaction by

S_{N} 1

Q. Explain the mechanism of esterification. Write the reactions involved in dehydration of

1^{o}

2^{o}

3^{o}

Q. Tertiary alkyl halides are particularly not substituted by

S_{N} 2

mechanism, because of:

View More

Join BYJU'S Learning Program

similar_icon

Related Videos

lock

Chemical Reactions of Amines

CHEMISTRY

Watch in App

explore_more_icon

Explore more

Formation of Diazonium Salts

Standard XII Chemistry

Join BYJU'S Learning Program

CrossIcon