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Vishal Baghel

Contributor-Level 10

Alkyl halides on treatment with sodium metal in dry ethereal (free from moisture) solution give higher alkanes. This reaction is known as Wurtz reaction and is used for the preparation of higher alkanes containing even number of carbon atoms.

For preparation of alkanes containing odd number of carbon atoms, a mixture of two alkyl halides has to be used. Since two alkyl halides can react in three different ways, therefore, a mixture of three alkanes instead of the desired alkane would be formed. For example, Wurtz reaction between 1-bromopropane and 1-bromobutane gives a mixture of three alkanes i.e., hexane, heptane and octane as shown

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Payal Gupta

Contributor-Level 10

3.46. (b) Electronegativity refers to the tendency of an atom to share electrons with another atom.

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Vishal Baghel

Contributor-Level 10

Anhydrous Ferric Chloride (FeCl3) is another Lewis acid which can be used during ethylation of benzene.

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Vishal Baghel

Contributor-Level 10

CH3 group is electron-donating while -NOgroup is electron-withdrawing. Therefore, maximum electron density will be in toluene, followed by benzene and least in m-dinitrobenzene. Therefore, the ease of nitration decreases in the order: toluene > benzene > m-dinitrobenzene.

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Vishal Baghel

Contributor-Level 10

(a) The typical reactions of benzene are electrophilic substitution reactions. Higher the electron-density in the benzene ring, more reactive is the compound towards thesereactions. Since NO2 is a more powerful electron-withdrawing group than Cl, therefore, more the number of nitro groups, less reactive is the compound. Thus, the overall reactivity decreases in the order:Chlorobenzene > p-nitrochlorobenzene > 2, 4-dinitrochlorobenzene

(b) Here, CH3 group is electron donating but NO2 group is electron-withdrawing. Therefore, the maximum electron-density will be in toluene, followed by p-nitrotoluene followed by p-dinitrobenzene. Thus,

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Payal Gupta

Contributor-Level 10

3.45.  (b) It has only ones-electron and hence can be placed in group 1 (alkali metals). It can also gain an electron to achieve a noble gas arrangement and hence it can behave similarly to a group 17 (halogen family) element. Because it is a special case, we shall place hydrogen separately at the top of the Periodic Table

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Vishal Baghel

Contributor-Level 10

The basic skeleton structure of 2-methylbutane is

Placing double bonds at different positions and satisfying the tetra covalency of each carbon, the structures of various alkenes which give 2-methylbutane on hydrogenation are: 

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New answer posted

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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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8 months ago

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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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