IDNLearn.com: Your go-to resource for finding expert answers. Our Q&A platform is designed to provide quick and accurate answers to any questions you may have.
Sagot :
yes this alcohol be synthesized selectively by hydroboration-oxidation of an alkene.
The initial hydroboration step determines the regioselectivity. Hydroboration proceeds in an antimarkovnikov manner. The reaction sequence is also stereoselective, giving syn addition (on the same face of the alkene): the hydroboration is syn-selective and the oxidation replaces the boron with hydroxyl having the same geometric position.
Thus 1-methyhexene reacts with diborane predominantly to give trans-1-hydroxy-2-methylhexene and the newly added H and OH are cis to each other.
CH3-CH2-CH2-CH2-C(CH3)=CH2
learn more about hydroboration-oxidation here:
https://brainly.com/question/2622427
#SPJ4
We appreciate every question and answer you provide. Keep engaging and finding the best solutions. This community is the perfect place to learn and grow together. Find reliable answers at IDNLearn.com. Thanks for stopping by, and come back for more trustworthy solutions.
