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How will you prepare benzene from...

How will you prepare benzene from

A

Benzene sulphonic acid

B

Phenol

C

Nitrobenzene

D

Benzoic acid

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The correct Answer is:
To prepare benzene from the given compounds (benzene sulfonic acid, phenol, nitrobenzene, and benzoic acid), we can follow these steps for each compound: ### 1. Preparation of Benzene from Benzene Sulfonic Acid **Step 1:** Start with benzene sulfonic acid (C6H5SO3H). **Step 2:** Treat benzene sulfonic acid with water (H2O) at a temperature of 150-200 °C in the presence of hydrochloric acid (HCl) and apply pressure. **Step 3:** The reaction will yield benzene (C6H6) and sulfuric acid (H2SO4) as a byproduct. **Chemical Equation:** C6H5SO3H + H2O → C6H6 + H2SO4 ### 2. Preparation of Benzene from Phenol **Step 1:** Start with phenol (C6H5OH). **Step 2:** React phenol with zinc dust (Zn) and heat the mixture. **Step 3:** This reaction will produce benzene (C6H6) and zinc oxide (ZnO) as a byproduct. **Chemical Equation:** C6H5OH + Zn → C6H6 + ZnO ### 3. Preparation of Benzene from Nitrobenzene **Step 1:** Start with nitrobenzene (C6H5NO2). **Step 2:** Reduce nitrobenzene using tin (Sn) and hydrochloric acid (HCl) to form aniline (C6H5NH2). **Step 3:** Treat aniline with sodium nitrite (NaNO2) and hydrochloric acid (HCl) to form benzene diazonium chloride (C6H5N2Cl). **Step 4:** Finally, hydrolyze benzene diazonium chloride using sodium hydroxide (NaOH) and cyanide chloride (ClCN) to yield benzene (C6H6). **Chemical Equation:** 1. C6H5NO2 + Sn + HCl → C6H5NH2 + SnCl2 2. C6H5NH2 + NaNO2 + HCl → C6H5N2Cl 3. C6H5N2Cl + NaOH + ClCN → C6H6 + byproducts ### 4. Preparation of Benzene from Benzoic Acid **Step 1:** Start with benzoic acid (C6H5COOH). **Step 2:** React benzoic acid with sodium hydroxide (NaOH) and heat to form sodium benzoate (C6H5COONa). **Step 3:** Perform a decarboxylation reaction by heating sodium benzoate with calcium oxide (CaO) to remove carbon dioxide (CO2) and yield benzene (C6H6). **Chemical Equation:** 1. C6H5COOH + NaOH → C6H5COONa + H2O 2. C6H5COONa + CaO → C6H6 + Na2CO3 + CO2 ### Summary In summary, benzene can be prepared from: - Benzene sulfonic acid via hydrolysis. - Phenol via reduction with zinc. - Nitrobenzene via reduction to aniline and subsequent diazotization. - Benzoic acid via decarboxylation of sodium benzoate. ---
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VMC MODULES ENGLISH-ALCOHOLS, PHENOLS & ETHERS-Enable
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  2. The major organic product in the reaction . CH(3) - O- CH (CH(3))(...

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  3. When HI reacts with diethyl ether in cold product would be :

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  4. Which of the following pairs will not form ether?

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  5. Phenol reacts with which of the following give bakelite ?

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  6. Which one of the following compounds is most acidic :-

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  7. C(6) H(5)NH(2) underset (0-5^(@))overset(HNO(2)//HCI)to X underset(H(2...

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  8. The correct order of increasing acidic strength is .

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  9. C(6)H(5) OH and C(6) H(5) COOH show difference in the reaction with

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  10. Phenol is heated with phthalic anhydride in the presence of conc. H(2)...

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  11. PhOH+CHCl(3) underset("Hydroxide")overset("Sodium")to product. The p...

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  12. Phenol is more acidic than :

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  13. Phenol gives . . . . . . . . Colour with neutral FeCl(3) solution :

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  14. What is the product formed in the following reaction? C(6)H(5)OH + "...

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  15. Asqirin is obtained by the reaction of salicylic acid with

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  16. The product of the reaction of phenol with bromine water is :

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  17. C(6)H(5)COCl+C(6)H(5)OH overset(NaOH)toC(6)H(5)COOC(6)H(5)+HCl This ...

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  18. In the avove reaction the intermediate species are :

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  19. How will you prepare benzene from

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  20. Phenol is acidic , because :

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