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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
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उत्तर
\[\begin{array}{cc}
\phantom{.}\ce{CH3}\phantom{...........................}\ce{CH3}\phantom{.........}\\
|\phantom{..............................}|\phantom{...........}\\
\ce{CH3 - C - CH2CH3 + HBr->[\Delta]CH3 - C - CH2CH3 + H2O}\\
|\phantom{..............................}|\phantom{...........}\\
\phantom{.}\ce{OH}\phantom{....................}\ce{\underset{2-bromo-2-methylbutane}{Br}}\phantom{..}\
\end{array}\]
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संबंधित प्रश्न
Intermolecular hydrogen bonding is strongest in ______.
Acidity of phenol is due to ____________.
The ionization constant of phenol is higher than that of ethanol because ____________.
Phenol reacts with Br2 in CS2 at low temperature to give ____________.

Strength of acidity is in order:

Which of the following compounds is most acidic?
Arrange the following in decreasing order of acidic character:

Which of the following statements is true:
Mark the correct order of decreasing acid strength of the following compounds.
| (a) | ![]() |
| (b) | ![]() |
| (c) | ![]() |
| (d) | ![]() |
| (e) | ![]() |
Assertion: o-Nitrophenol is less soluble in water than the m- and p-isomers.
Reason: m- and p- Nitrophenols exist as associated molecules.
Phenol is used in the manufacture of
Arrange the following in the increasing order of their property indicated:
4-Nitrobenzoic acid, benzoic acid, 3,4-Dinitrobenzoic acid, 4-Methoxy benzoic acid (Acid strength)
For the pair phenol and cyclohexanol, answer the following:
Why is phenol more acidic than cyclohexanol?
Give the structure of the product you would expect when the following alcohol reacts with HCl–ZnCl2.
2-Methylbutan-2-ol
Give the structure of the product you would expect when the following alcohol reacts with HBr.
Butan-1-ol
Give the structure of the product you would expect when the following alcohol reacts with SOCl2.
Butan-1-ol





