Answer :

Answer:

Option I. E2 and SN1

Explanation:

First, let's discard the options.

Option II cannot be because sodium ethoxide, although is a good nucleophyle, it's also a strong base, so it can take place a acid base reaction, and ethoxide act as base to substract an electrophyle from the iodohexane, therefore, it can go through a mechanism of elimination.

Option III cannot be either because the above explanation. Also a reaction in basic conditions can actually go through bimolecular reactions, so it has to be E2 only. E1 is in acidic conditions mostly and involves a carbocation, which in basic medium cannot be.

Because of the above explanation, option IV cannot be either.

Technically option 1 cannot be either because a reaction if it's bimolecular, then it has to be Sn2 and E2 only.

but it's the only option that has sense above all.

The mechanism is as follow:

${teks-lihat-gambar} joetheelite

The branch of science which deals with chemicals and bonds is called chemistry.

The correct option is A

The other option is wrong because of the following reason:-

  • Option II is wrong because sodium ethoxide, although it is a good nucleophile and also a strong base, so can take place in an acid-base reaction, and ethoxide acts as a base to subtract an electrophile from the isohexane, therefore, it can go through a mechanism of elimination.
  • Option III cannot be either because of the above explanation. Also, a reaction in basic conditions can actually go through bimolecular reactions, so it has to be E2 only. E1 is in acidic conditions mostly and involves a carbocation, which in the basic medium cannot be.

Hence, the correct option is 1 that is E2 +SN1

For more information, refer to the link:-

https://brainly.com/question/19524691