Haloalkanes and Haloarenes
Which of the following can give a Grignard reagent when reacted with magnesium in dry ether ?
Grignard reagent is usually prepared by : $$R-X+Mg\xrightarrow {E{ t }_{ 2 }O} RMgX$$ Grignard reagent $$Ar-X+Mg\xrightarrow {E{ t }_{ 2 }O} ArMgX$$ Grignard reagent Grignard reagent acts as a strong base. Grignard reagent carry out nucleophilic attack in absence of acidic hydrogen. Grignard reagent form complex with its ether solvent. Complex formation with molecule of ether is an important factor in the formation and stability of Grignard reagent. Which of the following Grignard reagents are not possible ?
(A)$$\overset {\delta +}{H}-S-CH_2CH_2CH_2-MgBr \xrightarrow [reaction]{acid-base} BrMgS-CH_2CH_2CH_3$$
(B) $$H-O-CH_2CH_2CH_2MgBr \xrightarrow [reaction]{acid-base} BrMgO-CH_2CH_2CH_3$$
(C) $$\overset {\delta +}{H}-\underset {|}{N}-CH_2CH_2-CH_2-MgBr \xrightarrow [reaction]{acid-base} BrMg-\underset {|}{N}-CH_2CH_2CH_3$$
$$\delta^+ H$$ $$H$$
So, all of these Grignard reagent can take their own acidic hydrogen. Therefore all of these Grignard reagents are not possible.
Which of the following can give a Grignard reagent when reacted with magnesium in dry ether ?
Provide the structure of compound $$A$$ in the following reaction.
The best yield of given product can be obtained by using which set of reactants $$X$$ and $$Y$$?
Which of the following does not form Grignard reagent on reaction with $$Mg$$ in the presence of ether?
An example of a sigma bonded organometallic compound is:
An allylide on hydrolysis gives allylene. The alkaline earth metal cation of allylide dissolves in dry ether in the presence of alkyl halide to form Grignard reagent. The allylide is :
In the following reaction, $$C_{6}H_{5}CH_{2}Br \underset {(ii)H_{3}O^{+}}{\xrightarrow {(i) Mg, Ether}} X$$, the product $$'X'$$ is:
The final product obtained in the reaction is:
Grignard reagent is prepared by the reaction between:
The best yield of given product can be obtained by using which set of reactants $$X$$ and $$Y$$?