Grignard reagents (RMgX, where R = alkyl/aryl, X = halogen) are highly reactive organometallic compounds used widely in organic synthesis.
Applications:
1. Synthesis of alcohols:
\[
\mathrm{R{-}MgX + CH_2O \;\longrightarrow\; RCH_2OMgX \xrightarrow{H_2O} RCH_2OH}
\]
(Formation of primary alcohol).
\[
\mathrm{R{-}MgX + R'CHO \;\longrightarrow\; RCH(OH)R'}
\]
(Formation of secondary alcohol).
\[
\mathrm{R{-}MgX + R'COR'' \;\longrightarrow\; R_3COH}
\]
(Formation of tertiary alcohol).
2. Formation of hydrocarbons:
\[
\mathrm{R{-}MgX + H_2O \;\longrightarrow\; RH + Mg(OH)X}
\]
3. Synthesis of carboxylic acids:
\[
\mathrm{R{-}MgX + CO_2 \;\longrightarrow\; RCOOMgX \xrightarrow{H_2O} RCOOH}
\]
Thus, Grignard reagents are versatile tools for forming C–C bonds and synthesising alcohols, hydrocarbons, and carboxylic acids.