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A compound X is formed by the reaction of a carboxylic acid C2H4O2 and an alcohol in presence of a few drops of H2SO4. The alcohol on oxidation with alkaline KMnO4 followed by acidification - Science

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प्रश्न

A compound X is formed by the reaction of a carboxylic acid C2H4O2 and an alcohol in presence of a few drops of H2SO4. The alcohol on oxidation with alkaline KMnO4 followed by acidification gives the same carboxylic acid as used in this reaction. Give the names and structures of

  1. carboxylic acid
  2. alcohol and
  3. the compound X.
    Also write the reaction.
संक्षेप में उत्तर

उत्तर

When ethanoic acid (C2H4O2) reacts with absolute ethanol (C2H6O) in the presence of an acid catalyst, the ester is formed. So, compound X is ethyl ethanoate. 

\[\ce{CH3COOH + CH3CH2OH -> \underset{Ester}{CH3COOC2H5} + H2O}\]

Ethanol on oxidation with alkaline KMnO4 gives ethanoic acid.

\[\ce{C2H5OH\overset{Alkaline  KmnO4}{ ->}CH3COOH}\]

  1. Ethanol on oxidation with alkaline KMnO4 gives ethanoic acid.
    \[\begin{array}{cc}
    \ce{H}\phantom{...}\ce{O}\phantom{....}\\
    |\phantom{....}||\phantom{....}\\
    \ce{H - C - C - O - H}\\
    |\phantom{.........}\\
    \ce{H}\phantom{.........}\\
    \end{array}\]
  2. Ethanol
    \[\begin{array}{cc}
    \ce{H}\phantom{....}\ce{H}\phantom{....}\\
    |\phantom{....}|\phantom{....}\\
    \ce{H - C - C - O - H}\\
    |\phantom{....}|\phantom{.....}\\
    \ce{H}\phantom{...}\ce{H}\phantom{.....}\\
    \end{array}\]
  3. Compound x is ethyl ethanoate (ester).
    \[\begin{array}{cc}
    \phantom{.........}\ce{H}\phantom{...}\ce{O}\phantom{.......}\ce{H}\phantom{...}\ce{H}\phantom{.........}\\
    |\phantom{....}||\phantom{........}|\phantom{....}|\\
    \ce{H - C - C - O - C - C - H}\\
    \phantom{.}|\phantom{.............}|\phantom{....}|\phantom{.}\\
    \phantom{.}\ce{H}\phantom{............}\ce{H}\phantom{...}\ce{H}\phantom{.}
    \end{array}\]
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अध्याय 4: Carbon and its Compounds - Short Answer Questions [पृष्ठ ३४]

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एनसीईआरटी एक्झांप्लर Science [English] Class 10
अध्याय 4 Carbon and its Compounds
Short Answer Questions | Q 33 | पृष्ठ ३४

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संबंधित प्रश्न

Fill in the following blank with suitable word:

Ethyne has ......... carbon-hydrogen single bonds.


Giving their structures, state the number of single bonds, double bonds and triple bonds (if any) in the following compounds:
ethyne


Write the molecular formula of  an alkene having 20 carbon atoms?


Which of the following hydrocarbons is unsaturated?
C3H4; C2H6


What happens when vegetable oils are hydrogenated? Name the catalyst used.


Which of the two is better for our health : butter or vegetable oil? Why?

 

Fill in the blanks and rewrite the completed statements:

The organic compounds having double or triple bond in them are termed as _________________   _________________.


Which among the following are unsaturated hydrocarbons?

  1. \[\ce{H3C - CH2 - CH2 - CH3}\]
  2. \[\ce{H3C - C ≡ C - CH3}\]
  3. \[\begin{array}{cc}
    \ce{H3C - CH - CH3}\\
    |\phantom{..}\\
    \ce{CH3}\\
    \end{array}\]
  4. \[\begin{array}{cc}
    \ce{H3C - C = CH2}\\
    |\\
    \phantom{...}\ce{CH3}\\
    \end{array}\]

Carbon, Group (14) element in the Periodic Table, is known to form compounds with many elements. Write an example of a compound formed with

  1. chlorine (Group 17 of Periodic Table)
  2. oxygen (Group 16 of Periodic Table)

Identify and name the functional groups present in the following compounds.

  1. \[\begin{array}{cc}
    \ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{..}\\
    \phantom{}|\phantom{....}|\phantom{....}|\phantom{..}\\
    \ce{H - C - C - C - OH}\\
    \phantom{}|\phantom{....}|\phantom{....}|\phantom{..}\\
    \ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{..}\\
    \end{array}\]
  2. \[\begin{array}{cc}
    \phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{....}\\
    \phantom{...}|\phantom{....}|\phantom{....}||\phantom{....}\\
    \ce{H - C - C - C - OH}\\
    \phantom{...}|\phantom{....}|\phantom{.........}\\
    \phantom{}\ce{H}\phantom{...}\ce{H}\phantom{.......}\\
    \end{array}\]
  3. \[\begin{array}{cc}
    \phantom{......}\ce{H}\phantom{....}\ce{H}\phantom{....}\ce{O}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{.......}\\
    \phantom{....}|\phantom{....}|\phantom{....}||\phantom{....}|\phantom{....}|\phantom{....}\\
    \ce{H} - \ce{C} - \ce{C} - \ce{C} - \ce{C} - \ce{C} - \ce{H}\\
    \phantom{....}|\phantom{.....}|\phantom{........}|\phantom{....}|\phantom{....}\\
    \phantom{....}\ce{H}\phantom{....}\ce{H}\phantom{........}\ce{H}\phantom{..}\ce{H}\phantom{.....}\\
    \end{array}\]
  4. \[\begin{array}{cc}
    \phantom{......}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{......}\\
    \phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}\\
    \ce{H - C - C - C = C - H}\\
    \phantom{....}|\phantom{....}|\phantom{.............}\\
    \phantom{....}\ce{H}\phantom{...}\ce{H}\phantom{.............}
    \end{array}\]

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