Hey guys, have a quick question.
Read the explanation, but it flipped the bromine so it's plane was on the page. This also moved all the other molecules to wedges and stuff and I just couldn't follow it...
Anyways, I put B because the methyl group being on the dash means that the hydrogen is on the wedge, which I thought was 180 degrees from the bromine and thus anti-periplanar. (Does this only work on cyclic rings such as cyclohexane?)
Can anyone help me visualize this besides changing the plane of everything unless that's absolutely what I have to do?
Read the explanation, but it flipped the bromine so it's plane was on the page. This also moved all the other molecules to wedges and stuff and I just couldn't follow it...
Anyways, I put B because the methyl group being on the dash means that the hydrogen is on the wedge, which I thought was 180 degrees from the bromine and thus anti-periplanar. (Does this only work on cyclic rings such as cyclohexane?)
Can anyone help me visualize this besides changing the plane of everything unless that's absolutely what I have to do?
