Explore topic-wise InterviewSolutions in Current Affairs.

This section includes 7 InterviewSolutions, each offering curated multiple-choice questions to sharpen your Current Affairs knowledge and support exam preparation. Choose a topic below to get started.

1.

Propanal-1 and pentan-3-one are the ozonolysis products of an alkene. What is th structural formula of alkene?

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`CH_(3)CH_(2)-underset(CH_(2)CH_(3))underset(|)(C)=CH-CH_(2)CH_(3)`
`CH_(3)CH_(2)-CH=CH-overset(CH_(2)CH_(3))overset(|)(C)H-CH_(3)`
`CH_(3)-underset(CH_(2)CH_(3))underset(|)(C)=overset(CH_(2)CH_(3))overset(|)(C)-CH_(3)`
`CH_(3)CH_(2)CH_(2)CH_(2)-CH=CH-CH_(2)CH_(3)`

SOLUTION :`CH_(3)CH_(2)-underset(CH_(3)-CH_(2))underset(|)(C)=O+O=underset(H)underset(|)(C)-CH_(2)-CH_(3) to CH_(3)-CH_(2)-underset(CH_(2)-CH_(3))underset(|)(C)=CH-CH_(2)-CH_(3)`
2.

Propanal and pentan-3-one are the ozonolysis products of an alkene ? What is the structural formula of the alkene ?

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Solution :(i)WRITE the structures of PROPANAL and pentan-3-one with their oxygen atoms facing each other. Remove oxygen atoms and join the TWO fragments by a DOUBLE bond, the structure of the alkene is
3.

Propanal and pentan-3-one are the ozonolysis products of an alkene? What is the structural formula of the alkene?

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SOLUTION :The PRODUCTS of OZONOLYSIS are
4.

Propan-1-ol can be prepared from propene by

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`H_(2)O //H_(2)SO_(4)`
`Hg(OAc)_(2)//H_(2)O` followed by `NaBH_(4)`
`B_(2)H_(6)` followed by `H_(2)O`
`CH_(3)CO_(2)H//H_(2)SO_(4)`

Solution :`6CH_(3)CH=CH_(2)+B_(2)H_(6) rarr 2(CH_(3)CH_(2)CH_(2))_(3)B UNDERSET(OH^(-))OVERSET(H_(2)O_(2))rarr 6CH_(3)CH_(2)CH_(2)OH+B(OH)_(3)`.
5.

Propan-1-ol and ethanol can be distinguished by

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LUCAS test
Iodoform test
Victor Meyer's test
All of these

Solution :Propan-1-ol does not RESPOND to iodoform test on reaction with `I_(2)` and `NAOH`.
6.

Propadiene overset(HCl(1eq))to A overset(O_2// LiAlH_4)to B + C (B and C are organic products ). If molecular mass of B is 32 then approximate molecular mass of C is

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98
68
58
46

Solution :A is 2-chloro PROPENE. B and C are
7.

Proof spirit contains about

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`40%` alcohol by weight
`50%` alcohol by weight
`25%` alcohol by weight
`10%` alcohol by weight

Solution :`49.3%` by weight.
8.

Proof spirit (by volume) is a mixture of

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`67.1%` ETHYL Alcohol `+32.9%` WATER
`95.87%` Ethyl Alcohol `+4.13%` Water
`57.1%` Ethyl Alcohol `+42.9%` Water
None of the above

Answer :C
9.

Prolonged oxidation of Ethane-1,2,-diol using periodic acid gives :

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ACETIC acid
Formic acid
Oxalic acid
Glyoxal

Solution :`{:(CH_(2)-CH_(2)),("|""|" overset(HIO_(4))rarr2HCHO),(OH""OH):}`
`UNDERSET("Further")(HCHO overset([O])RARR HCOOH)`
10.

Prof. Jonh gave a task to synthesize to three of his stundent ali, divakar and micheal. Difference routes were adopted by them. Ali's method Which of the following statements is correct?

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Ali and DIVAKAR will GET DESIRED product but YIELD will be better in divakar method
Ali and Micheal will get desired product but yield will be better in micheal method
Only micheal will get desired product
All of them will get desired product.

Answer :B
11.

Products. The total number of pi bonds in the products is

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SOLUTION :NUMBER of `pi` BONDS is 7 on PRODUCT 'X''
12.

Products of the following reaction Me_2C=CHCH_3 underset((ii)(CH_3)_2S)overset((i)O_3)to ? Are

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`CH_3CHO+CH_3COOH`
`Me_2CO+ CH_3CHO`
`Me_2CO+ CH_3COOH`
`2 Me_2CO`

Solution :`(CH_3)_2S` is USED for DECOMPOSITION of OZONIDES to give almost pure products .
13.

Products obtained in above Wurtz reaction is/are .

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SOLUTION :
14.

Products is

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SOLUTION :(d)CANNIZARO REACTION
15.

products formed are ?

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SOLUTION :
is ATTACKED at POSITION ANDC is FORMED
16.

products formed are

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SOLUTION :
17.

Products A and B formed in the following reactions are respectively:

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SOLUTION :N//A
18.

Products = ?

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SOLUTION :ALDOL CONDENSATION.
19.

Product will be

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Both A and B

Answer :C
20.

Product/s. The products formed are

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`CH_3 - OVERSET(O)overset(||)C-COOH`
`HOOC - COOH`
`CH_3-overset(O)overset(||)C-overset(O)overset(||)C-COOH`
Both (1) and (2)

Solution :`CH_3 C - overset(O)overset(||)C-COOH and HOOC - COOH`
21.

Product of the reaction is

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RACEMIC
Diastereomers
MESO
PURE enantiomers

SOLUTION :Racemic
22.

Product of the given reaction CH_(3)-CH=CH-Choverset(O_(3)//CH_(2)Cl_(2))underset(-78^(@)C)rarr will be :

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`CH_(3)-CHO`
`CH_(3)-COOH`
`CH_(3)-underset(OH)underset("|")"CH"-underset(OH)underset("|")"CH"-CH_(3)`

SOLUTION :
23.

Product of the reaction is

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`(CH_(3))_(2)C=CH_(2)`

Solution :NITRATION mixture gives `NO_(2)^(+)` as a ELECTROPHILE.
Tert-Butyl group was replaced by `NO_(2)`, then it makes benzene ring as deactivating group.
24.

Product of the Clemmensen reduction is ,

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ANSWER :3
25.

Product of addition of HBr on the alkene C_(6)H_(5) - CH = CH - CH_3 is

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`C_6H_5-UNDERSET(BR)underset(|)(CH)-CH_2-CH_3`
`C_6H_5-CH_2-underset(Br)underset(|)(CH)-CH_3`
`C_6H_5-CH_2-CH_2-CH_2-Br`
`Br-C_6H_4-CH_2-CH_2-CH_3`

ANSWER :A
26.

Product of above reaction is :

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ANSWER :B
27.

Product obtained in above reaction is :

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`3CH_(3)CHO`
`3HCHO`
`3HCOOH`
`3CH_(3)OH`

ANSWER :B
28.

Product obtained in above reaction are :

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ANSWER :D
29.

…………product obtained from the chlorination of benzene sulphonic acid in presence of FeCl_(3).

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SOLUTION :m CHLOROBENZENE sulphonic ACID.
30.

product not dormed is

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Solution :After ozonolysis base attacksmore acidic HYDROGEN forming CARBANION. NUCLEOPHILE created ATTACKS carbonyl carbon.
31.

Product M cannot respond with :

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2,4 -DNP
AMMONICAL SILVER nitrate
Sodium hypoiodite
Sodium bicarbonate

Answer :D
32.

product is

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SOLUTION :
33.

Product is:

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ANSWER :`(##RES_CHM_ROHR_E01_019_A01##)`
34.

Product formed is

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SOLUTION :
35.

Product formed on heating Pb(NO_(3))_(2) are

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`PBO,N_(2),O_(2)`
`Pb(NO_(2))_(2),O_(2)`
`PbO,NO_(2),O_(2)`
`Pb,N_(2),O_(2)`

Solution :`Pb(NO_(3))_(2)toPbO+NO_(2)+O_(2)`
36.

Product can be

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Solution :(A),(B),(C ),(D)
Due to Aldol CONDENSATION as WELL as dispropornation REACTION.
37.

Product ( C ) of the reaction is

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SOLUTION :
(SALT of `BETA`-KETOACID)
38.

Product (C) is

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ANSWER :B
39.

Product C is :

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ANSWER :D
40.

Product (B) in this reaction is ,

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SOLUTION :
CYCLOPENTANONE
41.

Product (A) undergoes how many stroctoral isomers ?

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Solution :
(2) those are (i) positinal isomers.(II) FUNCTIONAL GROUP isomerism.
42.

Product (A) is not ?

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SOLUTION : is OBTAINED
43.

Product (A) is:

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Solution :Once a SMALL amount of `OsO_(4)` is used up the `Os(VI)` by product is oxidized with is the reaction MIXTURE by the amine oxide acts as the ultimate OXIDANT.
44.

product A is :

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SOLUTION :
(L.D.A = LITHIUM di Isopropyl Amide)
L.D.A is sterically hindred BASE, so removes proton from less SUBSTITUTED `alpha-c` of ketone
45.

Product (A) is ,

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Solution :In basic medium halide UNDERGO elimination reaction(`E_(2)`ELIMANATION BIMOLECULAR)
46.

product (A) and (B) in above reactionis :

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`O^(_)-overset(O)overset(||)S-O-H,O^(-)-overset(O)overset(||)S-O-CH_(3)`
`O^(_)-overset(O)overset(||)S-O-H,O^(-)-""_(o+)underset(O^(-))underset(|)overset(O)overset(||)S-O-CH_(3)`
`O^(_)-overset(O)overset(||)S-O-CH_(3),O^(THETA)-""^(o+)underset(CH^(3))underset(|)overset(O)overset(||)S-H`
`O^(-)-""^(o+)underset(H)underset(|)overset(O)overset(||)S-O,O^(-)-underset(CH_(3))underset(|)overset(O)overset(||)S-O^(-)`

Solution :
( sulphur is better nucleophoile than OXYGEN )(but oxygen is better base than sulhur)
(A) Is FORMED by ACID -base reaction therefore oxygen will REACT.
(B) oid formed by electrophioe and nueophile reaction therefore sulphur wuill react.
47.

product

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SOLUTION :Clemmensons REDUCTION
48.

Which of the following method of separation can be applied to the mixture of liquids having different boiling points ?

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SIMPLE DISTILLATION
FRACTIONAL distillation
CRYSTALLIZATION
Fractional crystallization

ANSWER :A
49.

Among the reactions, F_(2(g)) + 2e^(-) to 2F_((g))^(-) and Cl_(2(g)) + 2e^(-) to 2Cl_((g))^(-) which is more feasible ? Give the reason.

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Solution :`F_(2(g)) + 2E^(-) to 2F_((g))^(-)` is easy.
Though electron gain ENTHALPY of `Cl_((g))` to give `Cl_((g))^(-)` is more than that of `F_((g))` to give the bond DISSOCIATION of `F_(2(g))` is very less than that of `Cl_(2(g))`.
50.

Process (A) : F_(2(g)) + 2e^(-) rarr 2F^(-)_((g)) , Process (B) : Cl_(2(g)) +2e^(-) rarr 2Cl_(g)^(-) which of these process is easy ? Why ?

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SOLUTION :`F_(2(g)) + 2e^(-) rarr 2F_((g))^(-)` is EASY.
Though electron GAIN enthalpy of `Cl_((g))` to give `Cl_((g))^(-)` is more thab that of `F_((g))`to give `F_((g))^(-)` , the bond dissociation of `F_((2(g)))` is very less than that of `Cl_(2(g))`