Seema Sinha Solutions for Chapter: Grignard Reagents and Organometallic Compounds, Exercise 1: DPP 1.1

$\underset{\mathrm{X}}{{\mathrm{C}}_{10}{\mathrm{H}}_{21}\mathrm{Br}}\underset{{\mathrm{H}}_3{\mathrm{O}}^{\oplus }}{\overset{\mathrm{Mg}}{\to }}\mathrm{Y}\stackrel{{\mathrm{Cl}}_2}{⟶}$ give $5$ types of structural monochloro products. $\mathrm{Y}$ has only $1°$ and $2°$ carbon atoms and $\mathrm{X}$ is $1°$ alkyl halide. Give structures of $\mathrm{X}$ and $\mathrm{Y}$.

Give the products for the viable reactions.

Analyse the following reaction: ${\mathrm{HOCH}}_2{\mathrm{CH}}_2{\mathrm{COCH}}_2{\mathrm{CH}}_2{\mathrm{CO}}_2\mathrm{Et}$

Which of the following compounds is formed by the reaction of sec-butylmagnesium iodide with a terminal alkyne?

$\mathrm{n}-$Propyl alcohol is obtained on hydrolysis of the adduct obtained by the reaction of:

Point out the incorrect Grignard reaction.

Which of the following statement(s) is/are true?

Which of the following reactions is/are not feasible?