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The compound ‘A’ having formula C8H(10) ...

The compound ‘A’ having formula `C_8H_(10)` (aromatic) which gives 1 mononitro substitute and 3 dinitrosubstitute compound is

A

m-xylene

B

p-xylene

C

o-xylene

D

Ethyl benzene

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The correct Answer is:
To solve the problem, we need to identify the compound 'A' with the formula \( C_8H_{10} \) that is aromatic and gives one mononitro substitution and three dinitro substitution products. ### Step-by-Step Solution: 1. **Identify the Structure**: The molecular formula \( C_8H_{10} \) indicates that the compound is likely an aromatic hydrocarbon. The degree of unsaturation can be calculated as follows: \[ \text{Degree of Unsaturation} = \frac{(2C + 2 - H)}{2} = \frac{(2 \times 8 + 2 - 10)}{2} = \frac{(16 + 2 - 10)}{2} = \frac{8}{2} = 4 \] This indicates that there are 4 rings or double bonds present in the structure, confirming that it is aromatic. 2. **Consider Possible Structures**: The compound could be a derivative of xylene. Xylene has the formula \( C_8H_{10} \) and exists in three isomeric forms: ortho-xylene, meta-xylene, and para-xylene. 3. **Analyze Substitution Patterns**: - **Mononitro Substitution**: When one nitro group is added, the compound can yield one mononitro product. This indicates that the compound must have a symmetrical structure that allows only one distinct position for the nitro group. - **Dinitro Substitution**: The compound can yield three different dinitro products. This suggests that there are three distinct positions available for the second nitro group after the first has been added. 4. **Identify the Correct Isomer**: - **Para-xylene** (1,4-dimethylbenzene) fits this requirement perfectly. When one nitro group is added to para-xylene, it can only go to one of the two methyl groups (yielding one mononitro product). - For dinitro substitution, the nitro groups can be placed in the following positions: 1. On one methyl group and the para position (1,4-dinitro). 2. On both methyl groups (2,5-dinitro). 3. On one methyl group and one of the hydrogen atoms adjacent to it (3,5-dinitro). 5. **Conclusion**: The compound 'A' is para-xylene (1,4-dimethylbenzene), which gives rise to one mononitro and three dinitro substitution products. ### Final Answer: The compound 'A' is **para-xylene (1,4-dimethylbenzene)**.

To solve the problem, we need to identify the compound 'A' with the formula \( C_8H_{10} \) that is aromatic and gives one mononitro substitution and three dinitro substitution products. ### Step-by-Step Solution: 1. **Identify the Structure**: The molecular formula \( C_8H_{10} \) indicates that the compound is likely an aromatic hydrocarbon. The degree of unsaturation can be calculated as follows: \[ \text{Degree of Unsaturation} = \frac{(2C + 2 - H)}{2} = \frac{(2 \times 8 + 2 - 10)}{2} = \frac{(16 + 2 - 10)}{2} = \frac{8}{2} = 4 ...
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ERRORLESS-HYDROCARBONS-NCERT BASED QUESTION (AROMATIC HYDROCARBON)
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  10. Reaction of benzene with Me(3)C COCl in the presence of anhydrous AlCl...

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  11. 1, 4-Dimethyl benzene on heating with anhydrous AICI(3)" and "HCI prod...

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  12. Identify the product (E) in the following sequence of reactions

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  13. Which of the following structures correspond to the product expected, ...

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  14. Friedel-Crafts acylation is-

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  15. In the following set of aromatic compounds the correct order of...

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  16. The major product obtained in the reaction of toluene with 1 - bromo-2...

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  17. The aromatic carbocation among the following is -

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  18. Among The compound which is not aromatic is

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  19. Among the following The antiaromatic compounds are

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