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V
Vishal Baghel

Contributor-Level 10

Benzene is a rich source of electrons because of the presence of an electron cloud containing 6 n-electrons above and below the plane of the ring. Consequently, it attracts the electrophiles (electron-deficient) reagents towards it and repels nucleophiles (electron- rich) reagents. As a result, benzene undergoes electrophilic substitution reactions easily and nucleophilic substitutions with difficulty.

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Payal Gupta

Contributor-Level 10

3.44.  (d) Assertion is a wrong statement. Non-metallic elements have a strong tendency to gain electrons. Therefore, electronegativity is directly related to those non-metallic properties of elements. It can be further extended to say that the electronegativity is inversely related to the metallic properties of elements.

Thus, the increase in electronegativities across a period is accompanied by an increase in non-metallic properties (or a decrease in metallic properties) of elements

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Vishal Baghel

Contributor-Level 10

The hybridization state of carbon in these three compounds is:

Since s-electrons are closer to the nucleus, therefore, as the s-character of the orbital making the C—H bond increases, the electrons of C—H bond lie closer and closer to the carbon atom. In other words, the partial +ve charge on the H-atom and hence the acidic character increases as the s-character of the orbital increases. Thus, the acidic character decreases in the order: Ethyne > Benzene > Hexane.

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Vishal Baghel

Contributor-Level 10

o-Xylene may be regarded as a resonance hybrid of the following two Kekule structures. Ozonolysis of each one of these gives two products as shown below:

Thus, in all, three products are formed. Since all the three products cannot be obtained from any one of the two Kekule structures, this shows that o-xylene is a resonance hybrid of the two Kekule structures (I and II).

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Vishal Baghel

Contributor-Level 10

Addition of HBr to propene is an ionic electrophilic addition reaction in which the electrophile, i.e., H+ first adds to give a more stable 2° carbocation. In the 2nd step, the carbocation is rapidly attacked by the nucleophile Br~ ion to give 2-bromopropane.

In presence of benzoyl peroxide, the reaction is still electrophilic but the electrophile here is a Br free radical which is obtained by the action of benzoyl peroxide on HBr.
In the first step, Br radical adds to propene to generate the more stable 2° free radical. In the second step, the free radical thus obtained rapidly abstracts a hydrogen atom from HBr to give 1-bromopr

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Vishal Baghel

Contributor-Level 10

Branching of carbon atom chain decreases the boiling point of alkane.

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Vishal Baghel

Contributor-Level 10

The expanded formula of the given compound is

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Payal Gupta

Contributor-Level 10

3.42. (a) Elements of the same group have similar valence shell electronic configuration and, therefore, exhibit similar chemical properties. However, the elements of the same period have an incrementally increasing number of electrons from left to right, and, therefore, have different valences.

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