Advertisements
Advertisements
प्रश्न
The formulae of four organic compounds are shown below. Choose the correct option
A | B | C | D |
\[\begin{array}{cc} \phantom{.}\ce{H}\phantom{......}\ce{H}\\ \phantom{.}\backslash\phantom{.....}/\\ \ce{C = C}\\ /\phantom{.....}\backslash\\ \ce{H}\phantom{......}\ce{H} \end{array}\] |
\[\begin{array}{cc} \phantom{........}\ce{H}\phantom{.....}\ce{O}\\ \phantom{.......}|\phantom{....}//\\ \ce{H - C - C}\\ \phantom{......}|\phantom{.....}\backslash\\ \phantom{...........}\ce{H}\phantom{.....}\ce{O - H} \end{array}\] |
\[\begin{array}{cc}
|
\[\begin{array}{cc} \ce{H}\phantom{...}\ce{H}\phantom{....}\\ |\phantom{....}|\phantom{....}\\ \ce{H - C - C - O - H}\\ |\phantom{....}|\phantom{.....}\\ \ce{H}\phantom{....}\ce{H}\phantom{.....} \end{array}\] |
विकल्प
A and B are unsaturated hydrocarbons
C and D are saturated hydrocarbons
Addition of hydrogen in presence of catalyst changes A to C
Addition of potassium permanganate changes B to D
उत्तर
Addition of hydrogen in presence of catalyst changes A to C
APPEARS IN
संबंधित प्रश्न
Draw the electron dot structures for F2.
You are given the following molecular formulae of some hydrocarbons:
C5H8; C7H14; C6H6; C5H10; C7H12; C6H12
Which two formulae represent unsaturated hydrocarbons having triple bonds?
Which of the following will give addition reaction and why?
C4H10, C2H6, C2H4, CH4, C3H8, C3H4
Differentiate between alkanes and alkenes. Name and draw the structure of one member of each.
Fill in the blanks and rewrite the completed statements:
The organic compounds having double or triple bond in them are termed as _________________ _________________.
Name a cyclic unsaturated carbon compound.
Which among the following are unsaturated hydrocarbons?
- \[\ce{H3C - CH2 - CH2 - CH3}\]
- \[\ce{H3C - C ≡ C - CH3}\]
- \[\begin{array}{cc}
\ce{H3C - CH - CH3}\\
|\phantom{..}\\
\ce{CH3}\\
\end{array}\] - \[\begin{array}{cc}
\ce{H3C - C = CH2}\\
|\\
\phantom{...}\ce{CH3}\\
\end{array}\]
Identify and name the functional groups present in the following compounds.
- \[\begin{array}{cc}
\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{..}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{..}\\
\ce{H - C - C - C - OH}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{..}\\
\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{..}\\
\end{array}\] - \[\begin{array}{cc}
\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{....}\\
\phantom{...}|\phantom{....}|\phantom{....}||\phantom{....}\\
\ce{H - C - C - C - OH}\\
\phantom{...}|\phantom{....}|\phantom{.........}\\
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{.......}\\
\end{array}\] - \[\begin{array}{cc}
\phantom{......}\ce{H}\phantom{....}\ce{H}\phantom{....}\ce{O}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{.......}\\
\phantom{....}|\phantom{....}|\phantom{....}||\phantom{....}|\phantom{....}|\phantom{....}\\
\ce{H} - \ce{C} - \ce{C} - \ce{C} - \ce{C} - \ce{C} - \ce{H}\\
\phantom{....}|\phantom{.....}|\phantom{........}|\phantom{....}|\phantom{....}\\
\phantom{....}\ce{H}\phantom{....}\ce{H}\phantom{........}\ce{H}\phantom{..}\ce{H}\phantom{.....}\\
\end{array}\] - \[\begin{array}{cc}
\phantom{......}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{......}\\
\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}\\
\ce{H - C - C - C = C - H}\\
\phantom{....}|\phantom{....}|\phantom{.............}\\
\phantom{....}\ce{H}\phantom{...}\ce{H}\phantom{.............}
\end{array}\]
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
- carboxylic acid
- alcohol and
- the compound X.
Also write the reaction.
Write the name of the following compound
\[\begin{array}{cc}
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{..}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{..}\\
\ce{H - C - C - C - C - C - OH}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{....}|\phantom{..}\\
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{..}
\end{array}\]