- AAcids
- BAmmonia
- CAlkanes
- DEsters
Explanation:
Amines are derivative of ammonia, wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group (these may respectively be called alkylamines and arylamines; in which both types of substituent are attached to one nitrogen atom may be called alkylarylamines).
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$F{e^{ + 3}}\left( {aq} \right) + {e^ - } \to F{e^{2 + }}\left( {aq} \right);{E^o} = + 0.77\,V$
$A{l^{ + 3}}\left( {aq} \right) + 3{e^ - } \to Al\left( s \right);{E^o} = - 1.66\,V$
$B{r_2}\left( {aq} \right) + 2{e^ - } \to 2B{r^ - };{E^o} = + 1.09\,V$
Considering the electrode potentials, which of the following represents the correct order of reducing power?
Reason : Fluorine has $2s^2\,2p^5$ configuration.

$(a)\;\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CCH}(\mathrm{OH}) \mathrm{CH}_{3} \stackrel{\mathrm{conc.H}, \mathrm{SO}_{4}}{\longrightarrow}$
$(b)\;\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CHCH}(\mathrm{Br}) \mathrm{CH}_{3} \stackrel{\text { alc.KOH }}{\longrightarrow}$
$(c)\;\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CHCH}(\mathrm{Br}) \mathrm{CH}_{3} \xrightarrow[\text { It should be }\left(\mathrm{CH}_{3}\right)_{3} \mathrm{CO}^{-} \mathrm{K}^{+}]{\text { given by } \mathrm{NTA}\left(\mathrm{CH}_{3}\right)_{3} \mathrm{O}^{-} \mathrm{K}^{+}}$
$(d)\;\begin{array}{*{20}{c}}
{{{(C{H_3})}_2}C - C{H_2} - CHO} \\
{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,} \\
{OH\,\,\,\,\,\,\,\,\,\,\,\,\,\,}
\end{array}\xrightarrow{\Delta }$
Which of these reaction(s) will not produce Saytzeff product ?