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Hint: We must remember that the Grignard reagent is a chemical compound having general formula R-Mg-X where X represents halogen atoms and R represents alkyl or aryl groups. Grignard reagent is used for the synthesis of hydrocarbon, alcohols, carboxylic acids etc.
Complete step by step answer:
We must know in the laboratory, Grignard reagent plays a major role in the synthesis of aldehydes from alcohol. In Grignard reagent, Mg metal is bonded with alkyl or aryl group by highly polar covalent bond and Mg bonded with halogen by ionic bond. Examples of Grignard reagents are methyl magnesium chloride $\left( {C{H_3}MgCl} \right)$, methyl magnesium bromide $\left( {C{H_3}MgBr} \right)$and phenyl magnesium bromide $\left( {{C_6}{H_5}MgBr} \right)$ which are collectively called as organo magnesium compound.
For the preparation of 2-methyl-propan-2-ol from methyl magnesium bromide, first we react the methyl magnesium bromide with propanone (having molecular formula${\text{C}}{{\text{H}}_3} - {\text{CO}} - {\text{C}}{{\text{H}}_3}$). When these two compounds reacts with each other they form an adduct having the following structure
After the formation of adduct we add water to the adduct, The water reacts with adduct results in the formation of Mg(OH)-Br and 2-methyl-propan-2-ol.
The balanced equation is given down below
${\text{C}}{{\text{H}}_3} - {\text{CO}} - {\text{ C}}{{\text{H}}_3}{\text{ + C}}{{\text{H}}_3} - {\text{MgBr }} \to {\text{ Adduct }} \to {\text{ Mg(OH)}} - {\text{Br + }}2 - methyl - propan - 2 - ol.$
Note:
We must remember that an Adduct is a direct product of a reaction which contains all the atoms of the reactants. When an adduct is being formed no other compound is being formed alongside an adduct which means that a single product is being achieved. An example of adduct is the addition of sodium bisulphate to an aldehyde which produces a sulphonate. Sulfonate contains both the aldehyde and sodium bisulphate.
Complete step by step answer:
We must know in the laboratory, Grignard reagent plays a major role in the synthesis of aldehydes from alcohol. In Grignard reagent, Mg metal is bonded with alkyl or aryl group by highly polar covalent bond and Mg bonded with halogen by ionic bond. Examples of Grignard reagents are methyl magnesium chloride $\left( {C{H_3}MgCl} \right)$, methyl magnesium bromide $\left( {C{H_3}MgBr} \right)$and phenyl magnesium bromide $\left( {{C_6}{H_5}MgBr} \right)$ which are collectively called as organo magnesium compound.
For the preparation of 2-methyl-propan-2-ol from methyl magnesium bromide, first we react the methyl magnesium bromide with propanone (having molecular formula${\text{C}}{{\text{H}}_3} - {\text{CO}} - {\text{C}}{{\text{H}}_3}$). When these two compounds reacts with each other they form an adduct having the following structure
After the formation of adduct we add water to the adduct, The water reacts with adduct results in the formation of Mg(OH)-Br and 2-methyl-propan-2-ol.
The balanced equation is given down below
${\text{C}}{{\text{H}}_3} - {\text{CO}} - {\text{ C}}{{\text{H}}_3}{\text{ + C}}{{\text{H}}_3} - {\text{MgBr }} \to {\text{ Adduct }} \to {\text{ Mg(OH)}} - {\text{Br + }}2 - methyl - propan - 2 - ol.$
Note:
We must remember that an Adduct is a direct product of a reaction which contains all the atoms of the reactants. When an adduct is being formed no other compound is being formed alongside an adduct which means that a single product is being achieved. An example of adduct is the addition of sodium bisulphate to an aldehyde which produces a sulphonate. Sulfonate contains both the aldehyde and sodium bisulphate.
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