Answer:
a. 3-methylbutan-2-ol
b. 2-methylcyclohexan-1-ol
Explanation:
For this reaction, we must remember that the hydroboration is an <u>"anti-Markovnikov" reaction</u>. This means that the "OH" will be added at the <em>least substituted carbon of the double bond.</em>
In the case of <u>2-methyl-2-butene</u>, the double bond is between carbons 2 and 3. Carbon 2 has two bonds with two methyls and carbon 3 is attached to 1 carbon. Therefore <u>the "OH" will be added to carbon three</u> producing <u>3-methylbutan-2-ol</u>.
For 1-methylcyclohexene, the double bond is between carbons 1 and 2. Carbon 1 is attached to two carbons (carbons 6 and 7) and carbon 2 is attached to one carbon (carbon 3). Therefore<u> the "OH" will be added to carbon 2</u> producing <u>2-methylcyclohexan-1-ol</u>.
See figure 1
I hope it helps!
Yes if you add an energy to an electron the electron will become excited, and it will jump to its highest level then go back down releasing energy
Based on this website I would say B. Hope this helps
Esters and Formation of esters. Esters and water are formed when alcohols react with carboxylic acids. This reaction is called esterification, which is a reversible reaction. ... Since esterification is a reversible reaction, esters can undergo hydrolysis to form corresponding alcohol and organic acid.
A. Radiation
Air in a car is heated up with the radiator and then blown out with an air pump.