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1.

In BHC, Benzene is chlorinated in the liquid phase in the presence of an activation agent, such as what?(a) Activating light(b) Gamma rays(c) Elemental fluorine(d) All of the mentionedThis question was posed to me during an interview for a job.My doubt stems from Halogenation in chapter Halogenation of Unit Processes

Answer»

The correct choice is (d) All of the mentioned

Explanation: BHC (Benzene Hexachloride or Hexachlorocyclohexane), in thisBenzene is chlorinated in the liquid PHASE in the presence of an ACTIVATION agent such as activating light, gamma RAYS, or elemental fluorine. A mixture of five ISOMERS of 1,2,3,4,5,6-hexachlorocyclohexane is produced .

2.

What is the formula of DDT?(a) 1,1,1-Trichloro-2,2-bis(p-chlorophenyl) ethane(b) 1,2,2-Trichloro-2,2-bis(p-chlorophenyl) methane(c) 1,1,1-Trichloro-2,2-bis(p-chlorophenyl) propane(d) None of the mentionedI have been asked this question in unit test.I'd like to ask this question from Halogenation topic in division Halogenation of Unit Processes

Answer»

The CORRECT ANSWER is (B) 1,2,2-Trichloro-2,2-bis(p-chlorophenyl) methane

Explanation: The FORMULA of DDT is: 1,1,1-Trichloro-2,2-bis(p-chlorophenyl) ETHANE.

3.

What is a Brine?(a) Coolant(b) Heat exchanger(c) Tower(d) ColumnThis question was posed to me in examination.This intriguing question comes from Halogenation topic in section Halogenation of Unit Processes

Answer» RIGHT answer is (a) Coolant

To explain I WOULD SAY: A Brine is a solution of NaCl, and is used as a coolant i.e. to REDUCE the temperature of the material.
4.

What do we get when Ethyl alcohol is chlorinated?(a) Alkyl(b) Hemiacetal(c) Azo(d) OximeThis question was posed to me by my school principal while I was bunking the class.My query is from Halogenation in division Halogenation of Unit Processes

Answer»

Right option is (b) Hemiacetal

For explanation I would SAY: Ethyl ALCOHOL either absolute or containing water is CHLORINATED to form the hemiacetal of TRICHLOROACETALDEHYDE from which chloral is liberated by treatment with concentrated sulfuric acid.

5.

What is meant by the Chlorination Catalysed by Active Carbon?(a) Promotes halogenation(b) Promotes hydrohalogenation(c) Promotes dehydrohalogenation(d) All of the mentionedI have been asked this question by my school teacher while I was bunking the class.This intriguing question originated from Halogenation in chapter Halogenation of Unit Processes

Answer»

The correct answer is (d) All of the mentioned

Easiest explanation: CHLORINATION CATALYSED by Active Carbon. When carbon of different densities is subjected to superheated steam, its surface is vaporized, forming capillaries which have the property of absorbing gases and compressing them into much SMALLER volumes. This COMPRESSION, possibly COMBINED with the catalytic effect of the metal impurities present in the carbon, promotes

6.

Which of the atoms has the capacity to form mixed halogens?(a) Fluorine(b) Bromine(c) Iodine(d) Both Br and II got this question in examination.I'd like to ask this question from Halogenation topic in chapter Halogenation of Unit Processes

Answer»

Right option is (d) Both Br and I

The best I can explain: Bromine and iodine, because of their capacity to form mixed HALOGENS, e.g., BrCI, BrFa, and ICI which have a low ENERGY of activation, are excellent halogenation catalysts. In general, it can be stated that small QUANTITIES of iodine and bromine are frequently ADDED ALONG

7.

What is the energy required to raise a molecule to a higher energy level?(a) Quantum(b) Exothermic energy(c) Work done(d) None of the mentionedThis question was addressed to me during an online interview.My question comes from Halogenation in portion Halogenation of Unit Processes

Answer»

Right OPTION is (a) QUANTUM

The explanation is: The amount of energy REQUIRED to raise a molecule to a HIGHER energy level is called a quantum. One of the factors that make up a quantum is a true energy value given i.e. ergs and called Planck’s constant, but the FORMULA for a quantum =h X constant/wavelength ( cm ).

8.

Which of the following compounds in contact with Fluorine are explosive in nature?(a) Benzene(b) Ether(c) Turpentine(d) All of the mentionedI got this question during a job interview.Question is from Halogenation in chapter Halogenation of Unit Processes

Answer»

Right answer is (d) All of the mentioned

To elaborate: Under atmospheric conditions, FLUORINE ATTACKS with violence all organic COMPOUNDS; benzene, ether, and turpentine take fire immediately on contact with it. Explanations of this violent and disruptive ACTIVITY that are in harmony with theoretical considerations.

9.

What is meant by photo halogenation?(a) Effect of electromagnetism(b) Reaction with wavelengths(c) All of the mentioned(d) None of the mentionedThe question was posed to me during an online interview.This interesting question is from Halogenation in portion Halogenation of Unit Processes

Answer»

The correct choice is (C) All of the mentioned

Explanation: PHOTO halogenation can be broadly defined as the effect of electromagnetic radiation on halogenation reactions and includes reactions which may be PRODUCED by all wavelengths from those of radio waves through x-rays, gamma rays, etc., into COSMIC rays.

10.

Antimony pentachloride is an excellent chlorine carrier.(a) True(b) FalseThis question was posed to me in an interview for internship.This is a very interesting question from Halogenation in division Halogenation of Unit Processes

Answer» RIGHT answer is (a) True

To explain: Antimony pentachloride is an excellent CHLORINE CARRIER. It has been USED extensively in the past for the manufacture of tetrachloroethane, ethylene dichloride, and tetrachlorophthalic anhydride, but most of these chlorination have been converted to ferric chloride procedures.
11.

In Aromatic Compounds Substitution, direct substitution of iodine into the benzene nucleus is feasible only in the presence of what?(a) Azo compound(b) Reducing agent(c) Oxidizing agent(d) None of the mentionedThis question was addressed to me in unit test.My query is from Halogenation topic in chapter Halogenation of Unit Processes

Answer» CORRECT answer is (c) Oxidizing agent

For explanation: In Aromatic Compounds Substitution, direct substitution of iodine into the benzene nucleus is FEASIBLE only in the presence of an oxidizing agent. The hydrogen iodide formed simultaneously with the iodo compound is UNSTABLE: the iodine in the benzene nucleus is loosely bound; and CONDITIONS must therefore be provided to AVOID reversibility.2C6H6 + I2 + (O) ——-> 2C6H5I + H2O.
12.

What is the name of the following reaction: CH3CH2Cl + KI ——-> CH3CH2I + KCl?(a) Addition reaction(b) Replacement reaction(c) Substitution reaction(d) Rearrangement reactionThe question was asked in semester exam.This is a very interesting question from Halogenation in portion Halogenation of Unit Processes

Answer»

Right ANSWER is (b) REPLACEMENT reaction

Easiest explanation: The above reaction is CALLED Replacement reaction because Iodine ATOM REPLACES Chlorine atom.

13.

Does physical and chemical factors have influence on peroxide molecules?(a) Yes(b) NoThis question was addressed to me in semester exam.The above asked question is from Halogenation in section Halogenation of Unit Processes

Answer»

Right answer is (a) Yes

For explanation I would say: The physical and chemical AGENCIES such as light, SOLVENT, and TEMPERATURE exert their peculiar influence on the peroxide molecules or in activating the OXYGEN liberated by the decomposition of the peroxides.

14.

Why is the bromination of the paraffin hydrocarbons is slower than chlorination?(a) Because it’s milder(b) It reacts faster(c) Highly reactive(d) None of the mentionedI had been asked this question during an interview.This key question is from Sandmeyer Reaction in section Halogenation of Unit Processes

Answer»

Correct ANSWER is (a) Because it’s milder

The best explanation: In general, methods similar to chlorination with chlorine and CHLORIDES can be employed in the preparation of bromine derivatives. Because the reaction is milder, the bromination of the paraffin hydrocarbons does not proceed so rapidly or to a GREAT degree; and with the LOWER permissible OPERATING temperature, the formation of polybromine compounds occurs to a lesser extent.

15.

Which type of reaction do we use for the production of Fluorobenzene ?(a) Sandmeyer’s reaction(b) Addition reaction(c) Substitution reaction(d) Rearrangement reactionThis question was addressed to me by my college director while I was bunking the class.This intriguing question originated from Sandmeyer Reaction topic in portion Halogenation of Unit Processes

Answer»

The CORRECT option is (a) Sandmeyer’s reaction

The explanation: The Sandmeyer reaction is a VALUABLE PROCEDURE for the preparation of halogen DERIVATIVES, such as fluorobenzene that generally cannot be made by other more direct METHODS.

16.

What is the name of the following reaction: C6H5-NH2-HCL + HF —–> C6H5-NH2-HF + HCl?(a) Addition reaction(b) Substitution reaction(c) Sandmeyer’s reaction(d) None of the mentionedThe question was asked during an interview.This intriguing question originated from Sandmeyer Reaction in portion Halogenation of Unit Processes

Answer»

The correct ANSWER is (c) Sandmeyer’s REACTION

For EXPLANATION I would SAY: The reaction is called Sandmeyer’s reaction because of the formation of DIAZONIUM solution, and sandmeyer’s reaction is used in formation of fluorination.

17.

In Sandmeyer reaction, what is the intermediate compound formed before adding cuprous halide?(a) Alcohol halide(b) Diazonium halide(c) Aqueous halide(d) None of the mentionedI have been asked this question during an interview.My doubt stems from Sandmeyer Reaction topic in section Halogenation of Unit Processes

Answer» RIGHT answer is (b) Diazonium halide

To explain I would say: During the reaction, FIRSTLY we prepare the SOLUTION of diazonium halide and gradually add it to a solution of the corresponding CUPROUS halide. Afterwards the diazotization and replacement of the diazo group TAKES place in one operation.
18.

What product do we get on chlorination of Fatty acids?(a) Alkyl chlorides(b) Acid chlorides(c) Chlorides(d) All of the mentionedThis question was addressed to me during a job interview.My doubt stems from Sandmeyer Reaction in section Halogenation of Unit Processes

Answer»

Correct choice is (b) Acid chlorides

Easiest explanation: Acid chlorides can be made from the corresponding fatty acids by TREATMENT with PHOSPHORUS halides such as : RCOOH + PCI5 ——-> RCOCl + POCL3 + HCI.

19.

Phosphorus pentachloride is employed as an esterification agent.(a) True(b) FalseI got this question during an interview for a job.This interesting question is from Sandmeyer Reaction topic in portion Halogenation of Unit Processes

Answer» CORRECT option is (a) True

To elaborate: It is true that Phosphorus pentachloride is EMPLOYED as an esterification agent in the treatment of alcohols, the HALIDE BECOMING hydrolysed during the REACTION.
20.

What do we get by chlorinating hydroxy or methoxybiphenyl?(a) Hydroxy hypochlorite(b) Aniline(c) Alkali hypochlorite(d) None of the mentionedI have been asked this question by my college director while I was bunking the class.This interesting question is from Sandmeyer Reaction topic in section Halogenation of Unit Processes

Answer»

The correct option is (c) Alkali HYPOCHLORITE

For EXPLANATION I would say: On chlorinating Alkali hypochlorite we GET hydroxy or methoxybiphenyl, the reaction is as FOLLOWS : C6H5-C6H5-OH ————–> C6H5-C6H5-Cl-OH.

21.

Which of the following is not a Chlorinating agent?(a) Thionyl Chloride(b) Sulfuryl Chloride(c) Phosphorus Chlorides(d) None of the mentionedI have been asked this question in an interview for job.The above asked question is from Sandmeyer Reaction topic in division Halogenation of Unit Processes

Answer» RIGHT OPTION is (d) None of the mentioned

Best EXPLANATION: Thionyl Chloride (SOCL2), Sulfuryl Chloride (SO2CL2) and Phosphorus Chlorides(PCL3, PCL5) are all USED as chlorinating agents.
22.

For the reaction of Alkyl chloride in presence of Alc.KOH gives what in product?(a) Alkyl(b) Alkene(c) Alcohol(d) None of the mentionedThe question was posed to me at a job interview.I would like to ask this question from Halogenation topic in portion Halogenation of Unit Processes

Answer»

The correct answer is (B) ALKENE

For EXPLANATION I would say: For EXAMPLE, when propylene DICHLORIDE is treated with an alcoholic solution of potassium hydroxide at ordinary temperatures, a-chloropropylene will be formed. Therefore in presence of Alcoholic KOH we convert Alkyl to Alkene (double bond).

23.

Alkyl halides and unsaturated aliphatic compounds cannot be simultaneously be obtained.(a) True(b) FalseI have been asked this question in unit test.The doubt is from Halogenation in division Halogenation of Unit Processes

Answer»

Correct choice is (b) False

The explanation: During Halogen Exchange reaction, the ALKYL halides and unsaturated aliphatic compounds can simultaneously be obtained by treating halogenated aliphatic carboxylic acids, NITRILES, or esters with aliphatic ALCOHOLS and/or ethers in the temperature range 260-320°0 and 700 lb PRESSURE. During the course of the reaction, HYDROGEN chloride is split out, the hydrogen and chlorine coming from adjacent carbon atoms. Under the conditions of reaction, the hydrogen chloride converts the reacting alcohol to the corresponding halide.

24.

In the reaction, Acetylene in presence of what give us Tetrachloroethane?(a) Zinc(b) HgCl2(c) FeCl2(d) Al2O3I got this question during an interview.The question is from Halogenation topic in chapter Halogenation of Unit Processes

Answer» CORRECT answer is (c) FeCl2

The best explanation: Acetylene in PRESENCE of FeCl2 give us TETRACHLOROETHANE, and this reaction is known as Halogenated olefins.
25.

CH2=CH2 + 2Cl2 + O2 ——–> _______ + 2H2O.Complete the following reaction?(a) CHCl=CHCl(b) CH2CL-CH2Cl(c) CH3-CH3(d) CCL3-CCL3I had been asked this question in a national level competition.This interesting question is from Halogenation in section Halogenation of Unit Processes

Answer»

The correct option is (a) CHCl=CHCl

To explain: CH2=CH2 + 2Cl2 + O2 ——–> CHCl=CHCL +2H2O, This REACTION is used for the PREPARATION of Chlorolefins, here we USE oxygen to convert any HYDROGEN chloride formed or introduced into active chlorine.

26.

What is meant by a Catalytic chamber?(a) Reactor(b) Quenching tower(c) Cooling tower(d) None of the mentionedThis question was addressed to me in class test.I'm obligated to ask this question of Halogenation in portion Halogenation of Unit Processes

Answer»

The correct ANSWER is (a) Reactor

Explanation: A CATALYTIC tower is a TYPE of a reactor tower, where catalytic reaction TAKES place.

27.

What do we get Chlorination of Carbon Disulphide?(a) Carbon Dichloride(b) Carbon Trichloride(c) Carbon Tetrachloride(d) None of the mentionedThe question was posed to me in my homework.This intriguing question originated from Halogenation in section Halogenation of Unit Processes

Answer»

Right answer is (C) Carbon Tetrachloride

The explanation is: CHLORINATION of Carbon Disulphide., the reaction is as follows CS2 + 3Cl2 —–> CCl4 + S2Cl2. , HENCE we GET Carbon Tetrachloride as product.

28.

Which type of chlorination is this reaction: CH3CHO + 3Cl2 ——->CCL3CHO + 3HCl ?(a) Chlorination of Alkali(b) Chlorination of Acetaldehyde(c) Chlorination of Ethanol(d) Chlorination of CycloparaffinsThe question was asked during an interview for a job.Origin of the question is Halogenation topic in portion Halogenation of Unit Processes

Answer»

Right answer is (B) Chlorination of Acetaldehyde

For explanation I WOULD say: Chlorination of Acetaldehyde. In some commercial processes for chloral, acetaldehyde, or its CONDENSATION product, paraldehyde is chlorinated under hydrous CONDITIONS.

29.

The Halogenated anthraquinones are derived from which reaction?(a) Friedel-Crafts reaction(b) Bechmann reaction(c) Olefins reaction(d) None of the mentionedI had been asked this question in my homework.This question is from Halogenation topic in section Halogenation of Unit Processes

Answer» RIGHT answer is (a) Friedel-Crafts REACTION

For EXPLANATION I would say: The halogenated anthraquinones are derived from the CORRESPONDING keto acids, which in turn are prepared according to the Friedel-Crafts reaction.
30.

What is the formula of Benzotrichloride?(a) C6H5-CCl3(b) C6H5-CHCl2(c) C6H5-CH2-Cl(d) C6H5-CH3I had been asked this question in an interview for internship.My doubt is from Halogenation and Its Types in portion Halogenation of Unit Processes

Answer»

Right option is (a) C6H5-CCl3

The best I can explain: BENZOTRICHLORIDE ACTS as a chlorinating AGENT, whose FORMULA is C6H5-CCl3.

31.

Is there a difference between Sandmeyer and Gattermann reaction?(a) Difference reaction temperature(b) Difference in pressure condition(c) Difference in catalyst(d) All of the mentionedI have been asked this question in an internship interview.My query is from Halogenation and Its Types in section Halogenation of Unit Processes

Answer» CORRECT CHOICE is (C) Difference in catalyst

Explanation: (HCl, Cu ) In Sandmeyer reaction : RN2Cl + Cu2Cl2 ———>RCL + N2 + Cu2Cl2Gattermann reaction:RN2CL ———–>RCl + N2.
32.

Thionyl Chloride is not a chlorinating agent.(a) True(b) FalseThe question was asked during an interview.My doubt stems from Halogenation and Its Types topic in section Halogenation of Unit Processes

Answer» CORRECT answer is (b) False

The best I can EXPLAIN: Thionyl Chloride- SOCL2 ACTS as a chlorinating AGENT.
33.

In which of the following reaction is Halogenation involved?(a) Addition(b) Substitution(c) Replacement(d) All of the mentionedThe question was asked in examination.The doubt is from Halogenation and Its Types in portion Halogenation of Unit Processes

Answer»

Right choice is (d) All of the mentioned

The explanation: halogenations may involve REACTIONS of (1) ADDITION, (2) SUBSTITUTION, Le. of hydrogen, (3) replacement, i.e., of groups, for example, the hydroxyl or sulfonic ACID group.

34.

Which derivative has pharmaceutical or dyeing properties?(a) Fluorine(b) Iodine(c) Bromine(d) ChlorineThe question was asked at a job interview.I want to ask this question from Halogenation and Its Types in division Halogenation of Unit Processes

Answer» CORRECT answer is (C) Bromine

To explain I WOULD say: The bromine derivative sometimes has certain advantages because of the greater EASE in effecting the replacement of this halogen in subsequent reactions or because it possesses certain PHARMACEUTICAL or dyeing properties.
35.

Which one of the following is the most important halogen in terms of preparations?(a) Bromine(b) Chlorine(c) Iodine(d) FluorineI have been asked this question in an internship interview.This question is from Halogenation and Its Types topic in section Halogenation of Unit Processes

Answer» RIGHT choice is (b) Chlorine

The explanation: The chlorine derivatives, because of the greater ECONOMY in effecting their preparation, are by far the most important of the technical halogen compounds and for this reason are given PRIMARY consideration. Chlorine > Bromine > IODINE > Fluorine.
36.

Which derivative is used for aerosol propellant?(a) Bromine(b) Chlorine(c) Iodine(d) FluorineThis question was addressed to me in an online quiz.This question is from Halogenation and Its Types in section Halogenation of Unit Processes

Answer»

The CORRECT answer is (d) Fluorine

The EXPLANATION is: The fluorine derivatives is well established in the FIELDS of refrigerants and aerosol propellants because of their stability and LOW boiling points.

37.

What is meant by Halogenation?(a) Introduction of Halogen atom(b) Removal of Halogen atom(c) Introduction & Removal of Halogen atom(d) None of the mentionedI got this question by my college professor while I was bunking the class.This key question is from Halogenation and Its Types topic in section Halogenation of Unit Processes

Answer» RIGHT choice is (a) Introduction of Halogen atom

The best EXPLANATION: Halogenation is DEFINED as the process where one or more halogen atoms are INTRODUCED into an ORGANIC compound.