Physical World
How many moles of ammonia will react with three moles of benzaldehyde to form osazone?
Which of the following is an example of nucleophilic addition to acetaldehyde?
Out of the four choices A, B and C are examples of nucleophilic additions. where as Choice D is an example of Reduction reaction.
Therefore the questions has three answers A, B, and C.
A nucleophilic addition reaction is an addition reaction where a chemical compound with an electron deficient or electrophilic double or triple bond, a π bond, reacts with electron-rich reactant, termed a nucleophile, with disappearance of the double bond and creation of two new single, or σ, bonds.
With a carbonyl compound as an electrophile, the nucleophile can be:
· An alcohol in acetalisation to an acetal.
· A cyanide anion in Cyanohydrin reactions forming a cyanohydrin product.
· A sulphur ion from sodium bisulfite which forms a bisulfite adduct with aldehyde groups.
The only type which is not a nucleophilic addition is the Wolff-Kishner reaction, which is the REDUCTION of aldehydes and ketones to alkanes.
How many moles of ammonia will react with three moles of benzaldehyde to form osazone?
How is 4-methylpent-3-en-2-one obtained from propan-e-one?
The reaction of $$C_6H_5CH=CHCHO$$ with $$LiAlH_4$$ gives.
Write the structures of the products of the given reaction: $$CH_3-CH_2-\underset{\underset{\,\,\,\,CH_3}{|}}CH_CHO\xrightarrow{NaBH_4}$$
Propose the mechanism for the following reaction: $$CH_3\ CHO+\ HCN \xrightarrow [ ]{ { H }_{ 2 } } \begin{matrix} { CH }_{ 3 }- & CH- & CN \\ & | & \\ & OH & \end{matrix}$$
The major product $$'Y'$$ in the following reaction is:
The only correct combination in which the reaction proceeds through radical mechanism is:
For the synthesis of benzoic acid, the only correct combination is:
Provide the structures of compounds A, B, C, and D in the above questions.
Provide the structures of compounds A, B, C, and D in the above questions.