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- Choose all compounds shown below (A-F) that can exist as pairs of cis-trans isomers: CH3CH2CH=C(CH3)2 CH3CH=C(CH3)CH2CH3 BrCH=CHCI CH2=CHCH3 C B D A OA Ов C D ОЕ OF BrCH2CH=CHCH2Br CH3CH=C(CH2CH3)2 E FWhat kind of isomerisation occur in the pairs a-f?Which pair of structures are enantiomers? COOH CH3 H HO HOOC OH CH3 H CH2CH3 Br H CH2CH3 Br cl H CH2CH3 CH3 H CH3 HO HO H CH2CH3 II, III I, II, III |, ||| I, II
- Starting from the Newman projection below, rotate the back carbon to provide the structure in the least stable conformation. (H3C)₂HC H Q IX H^ H H CH3 oPlease show reaekson and don't use hend raitingFollowing is the Structural formal of Chloropropane H H H 2. H Draw Newman projections for all staggered and eclipsed conformation formed by rotation about C1 - C2 bond from 0° to 360°. b) Which Staggered conformation(s) has the lowest energy; which has the highest energy? c) Which eclipsed conformation(s) has the lowest energy, which has thhe highest energy?
- 2. Convert the following bond-line structure to Newman projections that represents it lowest energy and highest energy conformations. Look down the indicated C2-C3 bond. lowest energy highest energyPlease don't provide handwriting solutionWhich of the following is the correct Newman projection for the following compound as viewed down the indicat conformation shown? CO II O III O IV OV CH3 CH3 CH31 CH3 CI || Br Br H CH3 CH3 ||| Br CH3 CH3 IV CI Br CH3