1.a.
1.b.
There are four isomers with the molecular formulaC4H9Cl. Only one of these isomers (compoundA) has a chiral center. When compound A is treated withsodium ethoxide, three products are formed: compounds B, C,and D. Compounds B and C arediastereomers, with compound B being the less stablediastereomer. Draw the structures forcompounds A, B, C, and D and label them.
Draw all four products that are expected when 2-ethyl-3-methyl-1,3-cyclohexadiene is treated with one equivalent of HBr at room temperature, and show mechanisms for their formation. For the mechanism, include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly. Do not use abbreviations such as Me or Ph. X Incorrect. Identify the locations where protonation can occur. Draw all four products.
1.a. 1.b. There are four isomers with the molecular formula C4H9Cl. Only one of these isomers (compound A) has a chiral
-
- Site Admin
- Posts: 899603
- Joined: Mon Aug 02, 2021 8:13 am