wiz-icon
MyQuestionIcon
MyQuestionIcon
1
You visited us 1 times! Enjoying our articles? Unlock Full Access!
Question

Product "x" major will be


A
No worries! We‘ve got your back. Try BYJU‘S free classes today!
B
No worries! We‘ve got your back. Try BYJU‘S free classes today!
C
Right on! Give the BNAT exam to get a 100% scholarship for BYJUS courses
D
No worries! We‘ve got your back. Try BYJU‘S free classes today!
Open in App
Solution

The correct option is C

The explanation for the correct option:

Option (C):

  1. When cyclohexene and bromine interact, 1,2-dibromocyclohexane is created.
  2. The process serves as the reaction of electrophilic addition. One bromine atom attaches to both carbon atoms during the initial phase of the process, with the bromine atom carrying the positive charge. An ion of bromine is created.
  3. A bromide ion then attacks the bromonium ion from behind due to a hindrance that the same side's bromine ion has produced.
  4. When ethanol is used to treat substituted cyclohexane, It then undergoes, nucleophilic substitution in presence of EtOH asEtO- acts as a nucleophile since it is a base.
  5. A nucleophile attacking a carbon atom with a partial positive charge is known as a nucleophilic substitution process. The nucleophile exchanges one atom that has a partial negative charge with another one.
  6. EtO-replace bromine attached at meta position by the SN1 reaction.
  7. An SN1 nucleophilic substitution process happens in two stages. The link between the carbon atom and the leaving group breaks in the first step, resulting in a carbocation and, most frequently, an anionic leaving group.
  8. The second stage includes the carbocation and nucleophile reaction to produce the substitution product.
  9. Hence, it is the correct option.

Therefore, x major will be


flag
Suggest Corrections
thumbs-up
0
Join BYJU'S Learning Program
similar_icon
Related Videos
thumbnail
lock
Reactions of Haloalkanes
CHEMISTRY
Watch in App
Join BYJU'S Learning Program
CrossIcon