Chemistry
Chemistry, 12.08.2021 22:20, garykids305

2-methyl-1-hexanol was prepared by reacting an alkene with either hydroboration-oxidation or oxymercuration-reduction. Draw the structure of the alkene that was used to prepare the alcohol in highest yield.
You do not have to consider stereochemistry.
You do not have to explicitly draw H atoms.
Indicate the method of preparation by drawing either BH3 (for hydroboration-oxidation), or Hg (for oxymercuration-reduction), in a separate sketcher.
If there is more than one alkene that can be used for a given method, draw all of them.
If either hydroboration-oxidation or oxymercuration-reduction can be used, just give the structures for one method.

answer
Answers: 2

Other questions on the subject: Chemistry

image
Chemistry, 21.06.2019 22:00, enrique2211
V1t2 = v2t1 is an expression of who’s law
Answers: 1
image
Chemistry, 21.06.2019 22:20, emilyborland50
Which of the following statements is false regarding aromaticity? a. the compound must be cyclic b. the compound must be fully conjugated c. the compound must be planar d. the number of electrons in the pi system must satisfy the hückel 4n+2 rule e. the compound must have a neutral charge
Answers: 2
image
Chemistry, 22.06.2019 09:40, loveoneonly9153
Consider this initial-rate data at a certain temperature for the reaction described by
Answers: 1
image
Chemistry, 22.06.2019 10:30, angemango3423
What is the empirical formula of c6h18o3? ch3o c2h5o c2h6o c2h5o5
Answers: 1
Do you know the correct answer?
2-methyl-1-hexanol was prepared by reacting an alkene with either hydroboration-oxidation or oxymerc...

Questions in other subjects:

Konu
Mathematics, 26.09.2019 12:50