Advertisements
Advertisements
प्रश्न
Give the structure of the product you would expect when the following alcohol reacts with HBr.
2-Methylbutan-2-ol
Advertisements
उत्तर
\[\begin{array}{cc}
\phantom{.}\ce{CH3}\phantom{...........................}\ce{CH3}\phantom{.........}\\
|\phantom{..............................}|\phantom{...........}\\
\ce{CH3 - C - CH2CH3 + HBr->[\Delta]CH3 - C - CH2CH3 + H2O}\\
|\phantom{..............................}|\phantom{...........}\\
\phantom{.}\ce{OH}\phantom{....................}\ce{\underset{2-bromo-2-methylbutane}{Br}}\phantom{..}\
\end{array}\]
APPEARS IN
संबंधित प्रश्न
Write the equation involved in the acetylation of Salicylic acid.
Give the structure of the product you would expect when the following alcohol reacts with HCl–ZnCl2.
Butan-1-ol
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.
Phenols do not react with one of the following:
Phenol is more acidic than alcohol because ____________.
Acidity of phenol is due to ____________.
The ionization constant of phenol is higher than that of ethanol because ____________.
In CH3CH2OH, the bond that undergoes heterolytical change most readily is ____________.
Phenol reacts with Br2 in CS2 at low temperature to give ____________.
Strength of acidity is in order:
Which of the following statements is true:
Mark the correct order of decreasing acid strength of the following compounds.
| (a) |  |
| (b) |  |
| (c) |  |
| (d) |  |
| (e) |  |
Out of o-nitrophenol and o-cresol which is more acidic?
Assertion: o-Nitrophenol is less soluble in water than the m- and p-isomers.
Reason: m- and p- Nitrophenols exist as associated molecules.
Which one of the following has the lowest pKa value?
Give the structure of the product you would expect when the following alcohol reacts with HCl–ZnCl2.
2-Methylbutan-2-ol
Compare acidity of phenol with that of ethanol.
