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प्रश्न
Give the structure of the product you would expect when the following alcohol reacts with HBr.
2-Methylbutan-2-ol
उत्तर
\[\begin{array}{cc}
\phantom{.}\ce{CH3}\phantom{...........................}\ce{CH3}\phantom{.........}\\
|\phantom{..............................}|\phantom{...........}\\
\ce{CH3 - C - CH2CH3 + HBr->[\Delta]CH3 - C - CH2CH3 + H2O}\\
|\phantom{..............................}|\phantom{...........}\\
\phantom{.}\ce{OH}\phantom{....................}\ce{\underset{2-bromo-2-methylbutane}{Br}}\phantom{..}\
\end{array}\]
संबंधित प्रश्न
Explain how does the −OH group attached to a carbon of benzene ring activate it towards electrophilic substitution?
Account for the following:
o-nitrophenol is more steam volatile than p-nitrophenol.
The product obtained from the reaction is:
Phenol is more acidic than alcohol because ____________.
Strength of acidity is in order:
Which of the following compounds is most acidic?
What is the correct order of reactivity of alcohols in the following reaction?
\[\ce{R-OH + HCl ->[ZnCl2] R-Cl + H2O}\]
Assertion: o-Nitrophenol is less soluble in water than the m- and p-isomers.
Reason: m- and p- Nitrophenols exist as associated molecules.
In the following compounds:
 |
 |
 |
 |
| (I) | (II) | (III) | (IV) |
The order to acidity is ______.
For the pair phenol and cyclohexanol, answer the following:
Why is phenol more acidic than cyclohexanol?
