Advertisements
Advertisements
Question
Write the final product(s) in each of the following reactions:
Solution
APPEARS IN
RELATED QUESTIONS
Write the mechanism of the following reaction:
Write the mechanism of the following reaction :
Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of the corresponding phenoxide ions.
Name the reagent used in the following reaction:
Oxidation of a primary alcohol to aldehyde.
When 3-methylbutan-2-ol is treated with HBr, the following reaction takes place:
\[\begin{array}{cc}
\phantom{.......................}\ce{Br}\\
\phantom{......................}|\\
\ce{CH3 - CH - CH - CH3 ->[HBr] CH3 - C - CH2 - CH3}\\
\phantom{.}|\phantom{......}|\phantom{......................}|\phantom{........}\\
\phantom{}\ce{CH3}\phantom{...}\ce{OH}\phantom{...................}\ce{CH3}\phantom{.....}
\end{array}\]
Give a mechanism for this reaction.
(Hint: The secondary carbocation formed in step II rearranges to a more
stable tertiary carbocation by a hydride ion shift from 3rd carbon atom.)
During dehydration of alcohols to alkenes by heating with cone. H2SO4 the initial step is ____________.
What is Lucas reagent?
What happens when (CH3)3 C – OH is heated with Cu/573 K?
Write the chemical equation in support of your answer.
Write the mechanism of acid dehydration of ethanol to yield ethene.
Write the mechanism of acid dehydration of ethanol to yield ethene.