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182.
\[\left( P \right)\xrightarrow[\Delta ]{EOH}\]
\[\left( Q \right)\xrightarrow[\Delta ]{EOH}Ph-C{{H}_{2}}-OH+Ph-C{{O}_{2}}\]
\[\left( R \right)\xrightarrow{{{O}_{3}}}P+Q,\] Structure of $$(R)$$ is:
183.
In this reaction,
$$C{H_3}CHO + HCN \to $$ \[C{{H}_{3}}CH\left( OH \right)CN\xrightarrow{H.OH}\] $$C{H_3}CH\left( {OH} \right)COOH$$
an asymmetric centre is generated. The acid obtained would be
Lactic acid obtained in the given reaction is an optically active compound due to the presence of chiral $$C$$ - atom. It exits as $$d$$ and $$l$$ - forms whose ratio is 1 : 1.
184.
Identify the products $$(X)$$ and $$(Y)$$ in the given reaction: \[\xrightarrow[AlC{{l}_{3}}]{{{\left( C{{H}_{3}}CO \right)}_{2}}O}X\xrightarrow[\text{conc}.\,{{H}_{2}}S{{O}_{4}}]{\text{conc}.\,HN{{O}_{3}}}Y\]
A
$$X =$$ Acetophenone, $$Y =$$ $$m$$ - Nitroacetophenone
B
$$X =$$ Toluene, $$Y =$$ $$m$$ - Nitroacetotoluene
C
$$X =$$ Acetophenone, $$Y = o$$ and $$p$$ - Dinitroacetophenone
D
$$X =$$ Benzaldehyde, $$Y =$$ $$m$$ - Nitrobenzaldehyde
Formaldehyde forms primary alcohol while all other aldehydes form secondary alcohols on reaction with Grignard's reagent followed by hydrolysis.
186.
An organic compound $$X$$ having molecular formula $${C_5}{H_{10}}O$$ yields phenyl hydrazone and gives negative response to the iodoform test and Tollen's test. It produces $$n$$ - pentane on reduction. $$X$$ could be
Since, the compound $$X$$ yields phenyl hydrazone and gives negative response to the iodoform test and Tollen's test , it must contain a $$C=O$$ group but is neither a methyl ketone nor an aldehyde. The structure of $$X$$ could be
having molecular formula $${C_5}{H_{10}}O.$$
187. \[\xrightarrow{{{H}^{+}}}X,\] most likely the compound $$X$$ is
Reaction of 4, 4 - dialkylcyclohexadienone with an acid to form phenol with the migration of one of the alkyl groups to the adjacent carbon is known as dienone-phenol rearrangement.
188.
Which compound is obtained when acetaldehyde is treated with dilute solution of caustic soda?
When formaldehyde is allowed to stand at room temperature, it slowly undergoes, polymerisation and forms a white solid called meta-formaldehyde or trioxane.