Consider the bromination of the compound 2-methyl 1-pentene in the attached file.
1. write the basic structure of the product of the bromination of 2-methyl 1-pentene, without regard to stereochemistry.
2. Does the product have any chiral carbons? If so, identify them with an circle.
3. How many stereoisomers are formed from the bromination of 2-methyl 1-pentene?
4. Draw Fischer projections of the stereoisomers formed in the bromination of 2-methyl 1-pentene and name each, including an "R" or "S" designation for the configuration of each stereoisomer.© BrainMass Inc. brainmass.com June 23, 2018, 3:26 pm ad1c9bdddf
Detailed description of finding the isomers of molecules. This entails finding the chiral centers and drawing fischer projections of molecules.