Answer:
See the explanation
Explanation:
In this case, we have to keep in mind that in the monosubstituted product we only have to replace 1 hydrogen with another group. In this case, we are going to use the methyl group
.
In the axial position, we have a more steric hindrance because we have two hydrogens near to the
group. If we have <u>more steric hindrance</u> the molecule would be <u>more unstable</u>. In the equatorial positions, we don't <u>any interactions</u> because the
group is pointing out. If we don't have <u>any steric hindrance</u> the molecule will be <u>more stable</u>, that's why the molecule will <u>the equatorial position.</u>
See figure 1
I hope it helps!
Answer:
Attached in the photo.
Explanation:
Hello,
The answers in the attached photo. Just three things:
- In the second point a parenthesis is missing to properly understand the molecule (after the oxygen), nevertheless, I assumed it was an ether.
- In the sixth point, there's a missing hydrogen for it to be an ether as well.
- In the tenth point the second parenthesis is not clear, it seems there's a missing subscript, nevertheless I draw it assuming complete octates.
Best regards.
No. The answer is false.
Just read that sentence aloud and you'll know that it does not sound right