Rotations around single bonds are allowed. Fischer projections are drawn in the eclipsed conformation.
Thank you for your answer.
- But, In the 'Staggered' configuration shown in the image the two Br atoms are oppositely(anti-addition on halogenation) placed.
- Now if I rotate this configuration so that I'm able to draw its Fischer projection I would be bringing closer the two Br atoms.
- For eg. If I rotate Carbon#3 about C2-C3 bond anti-clockwise so that C-3 Hydrogen is opposite to C-2's Br atom, The Br's would be closer than before.
So, would it not defy the anti-addition reaction mechanism of halogenation on alkene ?
Moreover, If I rotate the compound even more so that the two
Br's are exactly face-to-face each other(By rotating the shown Newman projection by 180deg) resulting conformation would be eclipsed and I'll be able to draw its Fischer projection but again,
Will it not defy the anti-addition reaction mechanism of halogenation on alkene?