In the following reaction, \(HC\equiv CH \overset { { H }_{ 2 }{ SO }_{ 4 } }{ \underset { HgS{ O }_{ 4 } }{ \longrightarrow } } X\) Product ‘X’ will not give _______.

Assertion: 2,2 – dimethyl propanoic acid does not give HVZ reaction.
Reason: 2 – 2, dimethyl propanoic acid does not have \(\alpha\) - hydrogen atom
Codes:
A) if both assertion and reason are true and reason is the correct explanation of assertion.
B) if both assertion and reason are true but reason is not the correct explanation of assertion.
C) assertion is true but reason is false
D) both assertion and reason are false

Which one of the following reduces tollens reagent

Which among the following on oxidation with alk.KMnO₄ will give butanone?

Which of the following acids do not exhibit optical isomerism?

Identify X and Y.
\({ CH }_{ 3 }CO{ CH }_{ 2 }{ CH }_{ 2 }COO{ C }_{ 2 }{ H }_{ 5 }\overset { { CH }_{ 3 }MgBr }{ \longrightarrow } X\overset { { H }_{ 3 }{ O }^{ + } }{ \longrightarrow } Y\)

What is angle of deviation due to reflection?

What happens when calcium acetate is dry distilled?

Arrange the following in increasing order of reactivity towards nucleophilic addition HCHO CH₃CHO and CH₃COCH₃

Benzaldehyde reduces Tollen's reagent but not Fehling's solution explain.

An alkene (A) on ozonolysis gives propanone and aldehyde (B). When (B) is oxidised (C) is obtained. (C) is treated with Br₂/P gives (D) which on hydrolysis gives (E). When propanone is treated with HCN followed by hydrolysis gives (E). Identify A, B, C, D and E.

A carbonyl compound A having molecular formula C₅H₁₀O forms crystalline precipitate with sodium bisulphate and gives positive iodoform test. A does not reduce Fehling solution. Identify A.

How is acetaldehyde prepared by the ozonolysis of CH₃CH=CHCH₃?

Formaldehyde and benzaldehyde give Cannizaro reaction but acetaldehyde does not - account for this.

How is carboxylic acid prepared from alcohols?

Write the structure of the major product of the aldol condensation of benzaldehyde with acetone.

Complete the following reaction
\({ CH }_{ 3 }-{ CH }_{ 2 }-{ CH }_{ 2 }-\underset { \overset { || }{ O } }{ C } -{ CH }_{ 3 }\overset { HO-{ CH }_{ 2 }-{ CH }_{ 2 }-OH }{ \underset { { dry }{ HCl} }{ \longrightarrow } } ?\)

Explain why carboxylic acids behave as acids. Discuss briefly the effects of electron withdrawing and donating substituents on acid strength of carboxylic acids.

An organic compound A (C₇H₆O) forms a bisulphite. A when treated with alcoholic KCN forms B (C₁₄H₁₂O₂) and A on refluxing with sodium acetate and acetic anhydride forms an add C (C₉H_sO₂). Identify A, B and C. Explain the conversion of A to B and C.