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प्रश्न
Find out all the functional groups present in the following polyfunctional compound.
Penicillin G, a naturally occurring antibiotic.
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उत्तर
Functional groups: Secondary amide \[\begin{array}{cc}\ce{O}\phantom{....}\\||\phantom{....}\\\ce{(-C-NH),}\end{array}\] carboxylic acid (–COOH), tertiary amide \[\begin{array}{cc}|\phantom{.....}\\\ce{- N - C -},\\\phantom{....}||\\\phantom{....}\ce{O}\end{array}\] thioether (R-S-R) groups are present in penicillin G.
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संबंधित प्रश्न
Draw a formula for the first five members of the homologous series beginning with the given compound.
CH3COCH3
Draw a formula for the first five members of the homologous series beginning with the given compound.
H–CH=CH2
Identify the functional group in the following compound.
Identify primary, secondary, tertiary, and quaternary carbon in the following compound.
\[\begin{array}{cc}\ce{CH3}\phantom{..................}\\
|\phantom{....................}\\\ce{CH3 - C - CH - CH2 - CH2 - CH3}\\|\phantom{.....}|\phantom{................}\\
\ce{CH3}\phantom{.}\ce{CH3}\phantom{..............}
\end{array}\]
Structure of the compound whose IUPAC name is 5, 6 – dimethylhept - 2 - ene is
Write a note on homologous series.
Write the molecular formula and possible structural formula of the first four members of homologous series of carboxylic acids.
Write the molecular formula of the first six members of homologous series of nitro – alkanes.
Identify the pair of organic compounds which belongs to homologous series.
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How many primary, secondary and tertiary carbon atoms respectively are present in isobutane?
Identify the number of carbon atoms and number of oxygen atoms respectively present in furan molecule.
An organic compound 'X' (molecular formula C6H7O2N) has six carbons in a ring system, two double bonds and also a nitro group as a substituent, 'X' is ______.
A pyranose ring consists of a skeleton of ______.
The correct decreasing order of priority for the functional groups of organic compounds in the IUPAC system of nomenclature is ______.
Identify primary, secondary, tertiary, and quaternary carbon in the following compound.
\[\begin{array}{cc}
\ce{CH3}\phantom{..................}\\
|\phantom{....................}\\
\ce{CH3 - C - CH - CH2 - CH2 - CH3}\\
|\phantom{....}|\phantom{................}\\
\ce{CH3} \ce{CH3}\phantom{..............}
\end{array}\]
Identify primary, secondary, tertiary and quaternary carbon in the following compounds.
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH - CH2 - CH2 - CH3}\\
\phantom{}|\phantom{....}|\phantom{...............}\\
\phantom{}\ce{CH3}\phantom{.}\ce{CH3}\phantom{.............}
\end{array}\]
Identify primary, secondary, tertiary and quaternary carbon in the following compound.
\[\begin{array}{cc}
\ce{CH3}\phantom{..................}\\
|\phantom{....................}\\
\ce{CH3 - C - CH - CH2 - CH2 - CH3}\\
|\phantom{....}|\phantom{................}\\
\ce{CH3}\phantom{..}\ce{CH3}\phantom{..............}\\
\end{array}\]
Identify primary, secondary, tertiary and quaternary carbon in the following compound.
\[\begin{array}{cc}
\ce{CH3}\phantom{..................}\\
|\phantom{....................}\\
\ce{CH3 - C - CH - CH2 - CH2 - CH3}\\
|\phantom{....}|\phantom{................}\\
\ce{CH3}\phantom{.}\ce{CH3}\phantom{..............}
\end{array}\]
Identify primary, secondary, tertiary and quaternary carbon in the following compound.
\begin{array}{cc}
\ce{CH3}\phantom{..................}\\
|\phantom{....................}\\
\ce{CH3 - C - CH - CH2 - CH2 - CH3}\\
|\phantom{....}|\phantom{................}\\
\ce{CH3}\ce{CH3}\phantom{..............}
\end{array}
Identify the α - carbons in the following species and give the total number of α-hydrogen in each.
\[\ce{CH3 - CH2 - \overset{\oplus}{C}H - CH2 - CH3}\]
Identify primary, secondary, tertiary and quaternary carbon in the following compound:
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{....................}\\
\ce{CH3 - C - CH - CH2 - CH2 - CH3}\\
|\phantom{....}|\phantom{................}\\
\ce{CH3}\phantom{.}\ce{CH3}\phantom{..............}\\
\end{array}\]
