Chemistry

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New answer posted

6 months ago

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R
Raj Pandey

Contributor-Level 9

p- toluenesulphonyl chloride

Only gives soluble product with alkali for 1° amine and for 2°- amine it gives insoluble product.

 

New answer posted

6 months ago

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R
Raj Pandey

Contributor-Level 9

Kindly consider the following Image 

 

New answer posted

6 months ago

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R
Raj Pandey

Contributor-Level 9

Kindly consider the following Image 

 

New answer posted

6 months ago

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R
Raj Pandey

Contributor-Level 9

OH group is the more activating group and ortho-para director, hence ortho position attach will provide meta substituted product with respect to – CH3 in option (C).

New answer posted

6 months ago

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A
Aadit Singh Uppal

Contributor-Level 10

Tautomerism is a dynamic equilibrium between 2 isomers, also known as tautomers, where a compound exists in 2 different structures. The most common form is keto enol tautomerism. It is mainly of two types:

  • Keto Form: Contains a C=O (carbonyl) group
  • Enol Form: Contains a C=C double bond and an –OH group

New answer posted

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V
Vishal Baghel

Contributor-Level 10

Tollen's reagent oxidises aldehydes into carboxylate ion whereas ketone is not oxidised by tollen's reagent.

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V
Vishal Baghel

Contributor-Level 10

Formation of Conjugated diene in option 3 make the given reactant most reactive towards dehydration in acidic conditions.

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V
Vishal Baghel

Contributor-Level 10

Reaction follows SN1 pathway involving Benzylic carbocation.

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Vishal Baghel

Contributor-Level 10

Ethylene diamine, en is bidentate, chelating ligand. Chelating ligands increase stability due to higher entropy factor.

New answer posted

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V
Vishal Baghel

Contributor-Level 10

The highest oxidation number corresponding to the group number in transition metal oxides is attained in Sc? O? to Mn? O? CrO is basic but Cr? O? is amphoteric.

Note: All the transition metals except scandium form MO oxides which are ionic (Only for 3d series, this statement is true)

Hence, (A), (C) and (D) are incorrect. But not given in the options.

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