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Amongest the following the most basic co...

Amongest the following the most basic compounds is-

A

p-nitro aniline

B

acetanilide

C

Aniline

D

Benzylamine

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The correct Answer is:
To determine which of the given compounds is the most basic, we need to analyze the structure and the electronic effects of each compound. Let's break it down step by step. ### Step 1: Identify the Compounds The four compounds provided are: 1. Para-nitroaniline 2. Acetanilide 3. Aniline 4. Benzylamine ### Step 2: Understand Basicity Basicity in organic compounds, especially amines, is primarily due to the availability of the lone pair of electrons on the nitrogen atom. The more available this lone pair is for donation, the stronger the base. ### Step 3: Analyze Each Compound - **Para-nitroaniline**: The presence of the nitro group (-NO2) is an electron-withdrawing group. This group pulls electron density away from the nitrogen, making the lone pair less available for donation. Thus, it decreases the basicity. - **Acetanilide**: In this compound, the nitrogen is bonded to a carbonyl group (C=O) and a methyl group (CH3). The carbonyl group also withdraws electron density from the nitrogen through resonance, which reduces the availability of the lone pair for donation. Therefore, it is less basic. - **Aniline**: Aniline has a lone pair on nitrogen that is partially delocalized into the aromatic ring due to resonance. This delocalization reduces the availability of the lone pair for protonation, making it less basic than expected. - **Benzylamine**: Benzylamine does not have any electron-withdrawing groups attached to the nitrogen. The lone pair on nitrogen is not involved in resonance with the aromatic ring, making it more available for donation. Thus, it is expected to be the most basic among the four. ### Step 4: Conclusion Based on the analysis, benzylamine has the most available lone pair for donation and is not affected by resonance or electron-withdrawing groups. Therefore, the most basic compound among the four options is **benzylamine**. ### Final Answer The most basic compound is **benzylamine** (option D). ---
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ALLEN-ACIDIC STRENGTH & BASIC STRENGTH-Exercise IV
  1. Which of the following is the strongest base:

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  2. Among the following acids, which has the lowest pK(a) value?

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  3. Amongest the following the most basic compounds is-

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  4. What is the conjugate base of OH^(-) ?

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  5. Among the following acids which has the lowest pk(a) value-

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  6. The correct order of increasing acid strength of the compounds is (a...

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  7. Which of these is the strongest base in aqueous media?

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  8. The correct order of increasing basicity of the given conjugate bases ...

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  9. The strongest acid amongst the following compounds is?

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  10. Arrange the following compounds in increasing order of acidity and giv...

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  11. In the following compounds: the order of basicity is as follows:

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  12. The most basic compound among the following is-

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  13. Most basic amine in the gas phase is :

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  14. Arrange the following compounds in order of decreasing acidity:

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  15. Conjugate base of hydrazoic acid HN(3) is :

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  16. Which among the following compounds will not give effervescence with s...

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  17. Considering the basic strength of amines in aqueous solution, which on...

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  18. Among the following oxoacids, the correct decreasing order of acid str...

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  19. Among the following compounds, the increasing order of their basic str...

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  20. The increasing order of basicity of the following compounds is

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