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Assertion: Amines are basic in nature. ...

Assertion: Amines are basic in nature.
Reason: Presence of ione pair of electron on nitrogenatom.

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**Step-by-Step Solution:** 1. **Understanding the Assertion:** The assertion states that "Amines are basic in nature." This means that amines can accept protons (H⁺ ions) and therefore act as bases according to the Brønsted-Lowry definition of acids and bases. **Hint:** Recall the definition of a base in the context of the Brønsted-Lowry theory. 2. **Understanding the Reason:** The reason provided is "Presence of lone pair of electrons on nitrogen atom." Nitrogen in amines has a lone pair of electrons which can be used to bond with protons. This property is what makes amines basic. **Hint:** Consider how the lone pair on nitrogen can interact with protons. 3. **Types of Amines:** Amines can be classified into primary (1°), secondary (2°), and tertiary (3°) amines based on the number of alkyl or aryl groups attached to the nitrogen atom. All types of amines exhibit basic properties due to the lone pair of electrons. **Hint:** Remember the structural differences between primary, secondary, and tertiary amines. 4. **Basicity Comparison:** While all amines are basic, there is a distinction between aliphatic (alkyl) amines and aromatic amines. Aliphatic amines are generally more basic than aromatic amines due to the delocalization of the lone pair in aromatic systems, which reduces its availability for bonding with protons. **Hint:** Think about how the structure of aromatic compounds affects electron availability. 5. **Conclusion:** Both the assertion and the reason are true. The presence of the lone pair of electrons on the nitrogen atom is indeed the reason why amines are basic. Therefore, the assertion and reason support each other. **Final Answer:** Both the assertion and reason are correct, and the reason is a correct explanation of the assertion.

**Step-by-Step Solution:** 1. **Understanding the Assertion:** The assertion states that "Amines are basic in nature." This means that amines can accept protons (H⁺ ions) and therefore act as bases according to the Brønsted-Lowry definition of acids and bases. **Hint:** Recall the definition of a base in the context of the Brønsted-Lowry theory. 2. **Understanding the Reason:** ...
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(a) If both assertion and reason are true and the reason is the correct explanation of the assertion of the assertion. (b) If both assertion and reason are true but reason is not the correct explanation of the assertion. (c) If assertion is true but reason is false. (d) If assertion is false but reason is true. Q. Assertion: Amines are basic in nature. Reason: Presence of lone pair of electrons on nitrogen atom.

Amines are basic in nature because-

Amines are basic in nature due to the presence of lone pair of electrons on N atom of -NH_(2) group. The basic strength of amines can be expressed by their dissociation constant, K_(b) or pK_(b) . RNH_(2) + H_(2) to R NH_(3)^(+) + OH^(-) K_(b) = ([RHH_(3)^(+)][OH^(-)])/([RNH_(2)]) and pK_(b) = -log K_(b) Greater the K_(b) value or smaller the pK_(b) value, more is the basic strength of amine. Aliphatic amines are stronger bases than ammonia due to the electron releasing effect of alkyl groups. The basic strength among amines decreases as : 2^(@) gt 1^(@) gt 3^(@) Aryl amines such as aniline are less basic than aliphatic amines due to the involvement of lone pair of electrons on N atom with the resonance in benzene. In derivatives of aniline, the electron releasing groups increase the basic strength while electron withdrawing groups decrease the basic strength. The base weakening effect of electron withdrawing group and base strengthening effect of electron releasing group is more marked at p-position than at m-position. Every o- substituted aniline is less basic than aniline due to ortho effect. Which of the following group does not decrease the basic strength of aniline ?

Amines are basic in nature due to the presence of lone pair of electrons on N atom of -NH_(2) group. The basic strength of amines can be expressed by their dissociation constant, K_(b) or pK_(b) . RNH_(2) + H_(2) to R NH_(3)^(+) + OH^(-) K_(b) = ([RHH_(3)^(+)][OH^(-)])/([RNH_(2)]) and pK_(b) = -log K_(b) Greater the K_(b) value or smaller the pK_(b) value, more is the basic strength of amine. Aliphatic amines are stronger bases than ammonia due to the electron releasing effect of alkyl groups. The basic strength among amines decreases as : 2^(@) gt 1^(@) gt 3^(@) Aryl amines such as aniline are less basic than aliphatic amines due to the involvement of lone pair of electrons on N atom with the resonance in benzene. In derivatives of aniline, the electron releasing groups increase the basic strength while electron withdrawing groups decrease the basic strength. The base weakening effect of electron withdrawing group and base strengthening effect of electron releasing group is more marked at p-position than at m-position. Every o- substituted aniline is less basic than aniline due to ortho effect. Which of the following statement is not correct?

Amines are basic in nature due to the presence of lone pair of electrons on N atom of -NH_(2) group. The basic strength of amines can be expressed by their dissociation constant, K_(b) or pK_(b) . RNH_(2) + H_(2) to R NH_(3)^(+) + OH^(-) K_(b) = ([RHH_(3)^(+)][OH^(-)])/([RNH_(2)]) and pK_(b) = -log K_(b) Greater the K_(b) value or smaller the pK_(b) value, more is the basic strength of amine. Aliphatic amines are stronger bases than ammonia due to the electron releasing effect of alkyl groups. The basic strength among amines decreases as : 2^(@) gt 1^(@) gt 3^(@) Aryl amines such as aniline are less basic than aliphatic amines due to the involvement of lone pair of electrons on N atom with the resonance in benzene. In derivatives of aniline, the electron releasing groups increase the basic strength while electron withdrawing groups decrease the basic strength. The base weakening effect of electron withdrawing group and base strengthening effect of electron releasing group is more marked at p-position than at m-position. Every o- substituted aniline is less basic than aniline due to ortho effect. The strongest base among the following is

ERRORLESS -NITROGEN CONTAINING COMPOUNDS -PREPARATION OF NITROGEN CONTAINING COMPOUNDS
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  2. Presently which reagent is used for separation of 1^(@),2^(@) and 3^(@...

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  3. Which of the following compounds is an amino acid

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  4. Rection of primary amines with aldehyde yields

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  12. Assertion: Nitrobenzene is used as a solvent in Friedel-Craft's reacti...

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  13. The electrolytic reduction of nitrobenzene in strongly acidic medium p...

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  14. The reaction CH(3)-underset(CH(3))underset(|)overset(CH(3))overset(|...

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  15. Consider the nitratio of benzene using mixed conc. H(2)SO(4) and HNO(3...

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  16. The correct statement regarding the basicity of arylamines is .

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