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Organic Chemistry problems

1.5 The alkene structure that upon ozonolysis-reduction yields CH3COCH3 + CH3CH2CHO is
a. CH3CH2CH2CH2CH=CH2
b. (CH3)2 C = C(CH3)2
c. (CH3)2CH2CH=CHCH3
d. (CH3)2C=CHCH2CH3

1.6 The best reagent to use to obtain 2-methyl-1-cyclohexanol from 1-methyl-1-cyclohexene is
a. H20 plus dilute acid
b. O3 followed by Zn, H30+
c. Hg(OAc)2 in water
d. BH3-THF followed by alkaline H2O2

1.7 Addition of Br2 to trans-3-hexene produces
a. a meso dibromide
b. a mixture of enantiomeric dibromides which is optically active
c. a mixture of enantiomeric dibromides which is optically inactive.
d. all of the above

Solution Preview

1.5 The provided reference gives detailed info on ozonolysis-reduction of alkenes. Basically the double bond in alkene will be broken and each attached with an oxygen. So the answer must be
D. ...

Solution Summary

The solutions provides detailed explanations, references and answer for the problem.

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