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9 months ago

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A
alok kumar singh

Contributor-Level 10

This is a Multiple Answer Type Questions as classified in NCERT Exemplar

The Correct option is c.

In the cyclic structure of glucose or fructose, anomeric carbon is carbon that is close to an oxygen atom. As shown in the structure above, atoms 'a' and 'b' are close to the oxygen atom, and the hydroxyl groups of both carbon atoms have different orientations.

New answer posted

9 months ago

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Vishal Baghel

Contributor-Level 10

This is a Multiple Choice Questions as classified in NCERT Exemplar

Ans: (B)

Among primary, secondary, and tertiary amines, tertiary amines are the most volatile compounds as they don't have any strong intermolecular H-bonding between N-H like the primary and secondary amines have. 

So due to weak dipole-dipole interactions, (B) will be the most volatile. 

New answer posted

9 months ago

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A
alok kumar singh

Contributor-Level 10

This is a Multiple Answer Type Questions as classified in NCERT Exemplar

The Correct option is a.

In the same way as (+) glyceraldehyde has a group on the lowest asymmetric carbon on the right side, the I, II, and III structures have a (-OH) group on the lowest asymmetric carbon on the right side giving them a D-configuration.

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Vishal Baghel

Contributor-Level 10

This is a Multiple Choice Questions as classified in NCERT Exemplar

Ans: (A)  

The basic strength of an atom is determined by its electron-donating capacity; in this case, the amide is the most basic due to the presence of a negative charge and two lone pairs of electrons on the nitrogen atom.

New answer posted

9 months ago

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alok kumar singh

Contributor-Level 10

This is a Multiple Answer Type Questions as classified in NCERT Exemplar

The Correct option is c.

The absence of a free (-CHO) aldehyde group is indicated by the fact that glucose pentaacetate does not react with hydroxylamine. The open structure of glucose cannot account for this, although the open chain structure of glucose can account for all other features.

New answer posted

9 months ago

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Vishal Baghel

Contributor-Level 10

This is a Multiple Choice Questions as classified in NCERT Exemplar

Ans: (D) 

Pyrrolidine is the strongest of two bases because the lone pair of nitrogen does not involve sin resonance, and the presence of two alkyl basic compounds increases the basic strength among the given four compounds.

New answer posted

9 months ago

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A
alok kumar singh

Contributor-Level 10

This is a Multiple Answer Type Questions as classified in NCERT Exemplar

Ans: The Correct option is a.

Anomers are cyclic monosaccharide structures that differ structurally at carbon-1. In this scenario, I and II are anomers since they differ only at carbon -1.

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9 months ago

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Vishal Baghel

Contributor-Level 10

This is a Multiple Choice Questions as classified in NCERT Exemplar

Ans:  (D) 

Since phenol is the strongest acid among the four options listed above, it is the weakest Brönsted base. The stronger the acid, the weaker the conjugate base.

Amines have a strong tendency to accept electrons thus they are a strong bronsted base while phenol is the strongest acid among all, therefore as per the relation of conjugative strong acids and weak bases, phenol is the weakest base. 

New answer posted

9 months ago

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alok kumar singh

Contributor-Level 10

This is a Multiple Answer Type Questions as classified in NCERT Exemplar

The Correct option is d.

Adenine, guanine, thymine, and cytosine are the four bases found in DNA. As a result, uracil is not found in DNA as we cannot identify it among the other nucleotides that are present in the DNA. Uracil is, however, seen in RNA, another nucleic acid found in most of the organisms.

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9 months ago

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Vishal Baghel

Contributor-Level 10

This is a Multiple Choice Questions as classified in NCERT Exemplar

Ans: (D)

Weak electrophile such as Diazonium cation readily reacts with electron-rich compounds which are having electron-rich compounds such as hydroxyl group, amino group. They don't react with electron-withdrawing groups like nitro groups. Therefore, nitrobenzene will not undergo an azo coupling reaction with benzene diazonium chloride. 

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