Answer: I think it's a don't blame me if it's wrong though
Explanation:
The answer is Big Mac size
<span>You have to use a Newman projection to make sure that the H on C#2 is anti-coplanar with the Br on C#1. (Those are the two things that are going to be eliminated to make the alkene.)
My Newman projection looks like this when it's in the right configuration:
Front carbon (C#2) has ethyl group straight up, H down/left, and CH3 down/right
Back carbon (C#1) has H straight down, Ph up/left, and Br up/right.
Then when you eliminate the H from C#2 and the Br from C#1, you will have Ph and the ethyl group on the same side of the molecule, and you'll have the remaining H and CH3 on the same side of the molecule.
This is going to give you (Z)-2-methyl-1-phenyl-1-butene.</span>
<span>When an electromagnetic wave passes from space to matter, some part of the energy is absorbed by the matter and it increases its energy. The wave may reflect and some part may pass through the matter depending on the amount of energy they have. The amplitude of the wave decreases if some parts of it are reflected. </span>
I think the answer is transparent and translucent
