Physical World
Which one of the following reagents reacts with both acetaldehyde and acetone?
Which among the following compounds will give a secondary alcohol on reacting with Grignard reagent followed by acid hydrolysis? I. $$HCHO$$ II. $$C_{2}H_{5}CHO$$ III. $$CH_{3}COCH_{3}$$ IV. $$RCOOC_{2}H_{5}$$ the correct option is:
Ketone and esters reacts with grignard reagent to give tertiary alcohols and aldehyde reacts with grignard to form secondary alcohols.The reaction with formaldehyde will produce primary alcohol
Which one of the following reagents reacts with both acetaldehyde and acetone?
The reaction of $${Me}_{3}C{Mg}Cl$$ and $${ Me }_{ 3 }C-\overset { O\\ \parallel }{ C } -C{ Me }_{ 3 }$$ after hydrolysis gives a gas $$(A)$$ and a $${2}^{o}$$ alcohol $$(B)$$ rather than the expected tri-t-butyl carbinol. Provide the structures of $$(A)$$ and $$(B)$$ with explanation.
Acetone on addition to methyl magnesium bromide forms a complex, which on decomposition with acid gives $$X$$ and $$Mg\left(OH\right)Br$$. Which one of the following is $$X$$?
Upon reaction with $$CH_3MgBr$$ followed by protonation, the compound that produces ethanol is:
What sequence of steps represents the best synthesis of 4-heptanol $${ \left( { CH }_{ 3 }{ CH }_{ 2 }{ CH }_{ 2 } \right) }_{ 2 }CHOH $$?
$$CH_{3}CH_{2}-\underset{\underset{Ph}{|}}{\overset{\overset{OH}{|}}{C}} - CH_{3}$$ cannot be prepared by:
The aldehydes which will not form Grignard product with one equivalent Grignard reagents are:
The correct sequences of reagents for the following conversation will be:
Reaction between acetone and methylmagnesium chloride followed by hydrolysis will give :
Considering all possible isomeric ketones, including stereoisomers of a compound having a molecular weight of $$100$$. All these isomers are independently reacted with NaBH$$_4$$. The total number of ketones that give a racemic product(s) is/are: [Note: stereoisomers are also reacted separately]