Carboxylic acids have higher boiling points than aldehydes,ketones,and even alcohols of comparable molecular mass. This is due to their:

  • A
    formation of intramolecular $H$-bonding
  • B
    formation of carboxylate ion
  • C
    more extensive association of carboxylic acid via van der Waals forces of attraction
  • D
    formation of intermolecular $H$-bonding

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Similar Questions

In the following reaction,$X$ and $Y$ respectively are:
$C_2H_5OH$ $\xrightarrow{KMnO_4 / H^+} X$ $\xrightarrow{C_2H_5OH / H_2SO_4, \Delta} CH_3COOC_2H_5$

$CH_3 - CH = CH - CH_2 - CO_2H \xrightarrow[\Delta ]{}(X) \,(major)$; Product $(X)$ is

Identify $X, Y$ and $Z$ in the following reaction sequence:
$C_6H_5CH_2CH_2OH$ $\xrightarrow{X} C_6H_5CH_2COOH$ $\xrightarrow{Y} Z$

Which of the following is most acidic?

Which among the following has the lowest boiling point?

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