Organic Chemistry Questions and Answers – Aryl Halides

This set of Organic Chemistry Multiple Choice Questions & Answers (MCQs) focuses on “Aryl Halides”.

1. Dehydrohalogenation of 1,2 di-bromo cyclohexane gives which of the following compound?
a)Dehydrohalogenation of 1,2 di-bromo cyclohexane - option a
b)Dehydrohalogenation of 1,2 di-bromo cyclohexane - option b
c)Dehydrohalogenation of 1,2 di-bromo cyclohexane - option c
d) Dehydrohalogenation of 1,2 di-bromo cyclohexane - option d
View Answer

Answer: a
Explanation: As we can see in below reaction that double E2 elimination yields the conjugated diene, 1,3-cyclohexadiene. Note the overall transformation is alkene to conjugated diene.
The overall transformation is alkene to conjugated diene

2. Which one of the following possess highest melting point?
a) Chlorobenzene
b) o-dichlorobenzene
c) m-dichlorobenzene
d) p-dichlorobenzene
View Answer

Answer: d
Explanation: p-dichlorobenzene molecule has symmetrical structure. It can fit well in its crystal lattice. The intermolecular forces of attraction are strong. Hence, it possesses highest melting point.

3. What would be the product formed for the following reaction?
a) The product formed for the following reaction 1-Bromo-3-chloro cyclobutane - option a
b) The product formed for the following reaction 1-Bromo-3-chloro cyclobutane - option b
c) The product formed for the following reaction 1-Bromo-3-chloro cyclobutane - option c
d) The product formed for the following reaction 1-Bromo-3-chloro cyclobutane - option d
View Answer

Answer: d
Explanation: When 1-Bromo-3-chloro cyclobutane reacts with two equivalents of metallic sodium in ether it is the example of Wurtz reaction.
1-Bromo-3-chloro cyclobutane reacts with two equivalents of metallic sodium in ether
advertisement
advertisement

4. Which of these can be used as moth repellent?
a) Benzene hexachloride
b) Benzal chloride
c) Hexachloroethane
d) Tetrachloroethane
View Answer

Answer: c
Explanation: Hexachloroethane can be used as moth repellent. It has also been used as a plasticizer for cellulose esters in place of camphor, a polymer additive, a component of fungicidal and insecticidal formulations, in the formulation of extreme pressure lubricants, and in the manufacture of fire extinguishing fluids.

5. What will be the product for the following reaction?
Find the product for the following reaction −CCl3
a) The product for the following reaction −CCl3 - option a
b) The product for the following reaction −CCl3 - option b
c) The product for the following reaction −CCl3 - option c
d) The product for the following reaction −CCl3 - option d
View Answer

Answer: a
Explanation: −CCl3 is a m-directing group. So, attack will be at meta position.
Note: Join free Sanfoundry classes at Telegram or Youtube

6. Which of the following is true about chlorobenzene?
a) Chlorobenzene is less reactive than benzyl chloride
b) Chlorobenzene is more reactive than ethyl bromide
c) Chlorobenzene is nearly as reactive as methyl chloride
d) Chlorobenzene is more reactive than isopropyl chloride
View Answer

Answer: a
Explanation: Chlorobenzene is less reactive than benzyl chloride. In chlorobenzene the lone pairs present on Cl atom get involved in resonance with π electrons of benzene due to which C−Cl bond acquires double bond character Hence, reactivity decreases. C2H5−Cl is more reactive than C6H5−CH2−Cl.

7. In the below process what is the product A?
The product A is Fluorobenzene treated with nitrous acid
a) Fluorobenzene
b) Benzene
c) 1, 4-difluorobenzene
d) 1, 3-difluorobenzene
View Answer

Answer: a
Explanation: In this reaction aniline is to be treated with nitrous acid to form benzene diazonium chloride, which is further reacted with HBF4 to form benzene diazonium fluorobarate. This is when heated, undergoes decomposition to give fluorobenzene. This reaction is called as Balz-Shiemann reaction.
advertisement

8. What is the name of the following reaction?
The name of the following reaction is Sandmeyer’s reaction with nucleophile
a) Chlorination
b) Sandmeyer’s reaction
c) Perkin reaction
d) Substitution reaction
View Answer

Answer: b
Explanation: The substitution of an aromatic amino group is possible via preparation of its diazonium salt and subsequent displacement with a nucleophile (Cl, I, CN, RS, HO) is known as Sandmeyer’s reaction.

9. Which of the following is the commercial method of preparation of Chlorobenzene?
a) Raschig process
b) Wurtz Fitting reaction
c) Friedel-Crafts reaction
d) Grignard reaction
View Answer

Answer: a
Explanation: An industrial process for making chlorobenzene (and phenol) by a gas-phase reaction between benzene vapour, hydrogen chloride, and oxygen (air) at 230°C. The catalyst is copper(II) chloride.
2C6H6 + 2HCl + O2 → 2H2O + 2C6H5Cl
advertisement

10. Benzene reacts with chlorine to form benzene hexachloride in presence of which of the following reactant?
a) Nickel
b) AlCl3
c) Bright sunlight
d) Zinc
View Answer

Answer: c
Explanation: Benzene will react with three molecules of chlorine in the presence of sunlight to give benzene hexachloride.

Sanfoundry Global Education & Learning Series – Organic Chemistry.

To practice all areas of Organic Chemistry, here is complete set of 1000+ Multiple Choice Questions and Answers.

If you find a mistake in question / option / answer, kindly take a screenshot and email to [email protected]

advertisement
advertisement
Subscribe to our Newsletters (Subject-wise). Participate in the Sanfoundry Certification contest to get free Certificate of Merit. Join our social networks below and stay updated with latest contests, videos, internships and jobs!

Youtube | Telegram | LinkedIn | Instagram | Facebook | Twitter | Pinterest
Manish Bhojasia - Founder & CTO at Sanfoundry
Manish Bhojasia, a technology veteran with 20+ years @ Cisco & Wipro, is Founder and CTO at Sanfoundry. He lives in Bangalore, and focuses on development of Linux Kernel, SAN Technologies, Advanced C, Data Structures & Alogrithms. Stay connected with him at LinkedIn.

Subscribe to his free Masterclasses at Youtube & discussions at Telegram SanfoundryClasses.