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Mixed Test (Chemistry)

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Which of the following statements is/are true? A. In column chromatography, the more highly absorbed component is eluted with less polar solvents. B. Benzoic acid can be extracted from water using ethanol. C. Number of replaceable hydroxyl ions present in one molecule of a base is called its acidity.

  1. Only A

  2. Only B

  3. Only C

  4. A and B

  5. B and C


Correct Option: C
Explanation:

This option is correct because number of replaceable hydroxyl ions present in one molecule of a base is called its acidity is true statement.

Assertion: The compound C6H5CH=CHCl is called β-chlorostyrene. Reason: In organic halides, the carbon atom attached to the halogen atom designated as α.

  1. Both A and R are true and R is the correct explanation of A.

  2. Both A and R are true but R is NOT the correct explanation of A.

  3. A is true but R is false.

  4. A is false but R is true.

  5. Both A and R are false.


Correct Option: B
Explanation:

This option is correct, because in styrene, carbon atom attached to phenyl group is designated as α-carbon while that carrying Cl-atom is designated as β-carbon.

Assertion: The CH2F2, the F-C-F bond angle is less than 109.5˚ indicating less than 25% s-character but the H-C-H bond angle is larger and the C-H bond has more s-character. Reason: More electronegative substituents prefer hybrid orbitals having less s-character and more electropositive substituents prefer hybrid orbitals having more s-character.

  1. Both A and R are true and R is the correct explanation of A.

  2. Both A and R are true but R is NOT the correct explanation of A.

  3. A is true but R is false.

  4. A is false but R is true.

  5. Both A and R are false.


Correct Option: A
Explanation:

This option is correct because according to bent rule more electronegative substituents prefer hybrid orbitals having less s-character and more electropositive substituents prefer hybrid orbitals having more s-character. An example of this rule is fluoromethanes.

Which of the following statements is/are correct? A. 1-chloro-2, 3-pentadiene has no chiral carbon atoms, yet it is a chiral molecule. B. A newly discovered compound is through to be chiral but shows no rotation in a specific solvent. Does this mean that the compound is assuredly achiral? C. When a chiral molecule reacts to give a chiral molecule, the product is always racemic.

  1. Only A

  2. Only B

  3. Only C

  4. Both A and C

  5. Both B and C


Correct Option: A
Explanation:

This statement is correct, because the molecule as whole is chiral, since this molecule and its mirror image are non-superimposable.

Assertion: Cyclohexane floats over water. Reason: Most of the molecules of cyclohexane assume boat conformation.

  1. Both A and R are true and R is the correct explanation of A.

  2. Both A and R are true but R is NOT the correct explanation of A.

  3. A is true but R is false.

  4. A is false but R is true.

  5. Both A and R are false.


Correct Option: C
Explanation:

This option is correct because cyclohexane floats over water is due to density of cyclohexane is lower than that of water.

Which of the following statements is/are wrong? A. 1-methoxypropane and 2-methoxyprpane are metamers. B. An optically inactive substance must be achiral. C. m-Chlorobromobenzene and m-bromochlorobenzene are isomers.

  1. Both A and B

  2. Both A and C

  3. Both B and C

  4. A, B, and C

  5. None of these


Correct Option: D
Explanation:

1-methoxypropane and 2-methoxyprpane are chain or position isomers, a racemic mixture shows no optical activity and m-chlorobromobenzene and m-bromochlorobenzene represents the same compound, so the statement A, B, and C all are incorrect. Thus, this option is correct.

Assertion: 1, 2-propadiene exhibits optical isomerism. Reason: Its mirror image is non-superimposable.

  1. Both A and R are true and R is the correct explanation of A.

  2. Both A and R are true but R is NOT the correct explanation of A.

  3. A is true but R is false.

  4. A is false but R is true.

  5. Both A and R are false.


Correct Option: E
Explanation:

This option is correct because 1, 2-propadiene does not exhibits optical isomerism due to it contains axis of symmetry.

Assertion: All the carbon atoms in but-2-ene lie in one plane. Reason: All the carbon atoms of but-2-ene are sp2-hybridized.

  1. Both A and R are true and R is the correct explanation of A.

  2. Both A and R are true but R is NOT the correct explanation of A.

  3. A is true but R is false.

  4. A is false but R is true.

  5. Both A and R are false.


Correct Option: C
Explanation:

This option is correct, because all the carbon atoms in but-2-ene lie in one plane and only carbon atoms of the double bond are sp2-hybridized.

Assertion: The energy difference between staggered and eclipsed conformations of ethylene dichloride is less than in ethylene dibromide. Reason: The bond moment of C-Cl is greater than that of C-Br.

  1. Both A and R are true and R is the correct explanation of A.

  2. Both A and R are true but R is NOT the correct explanation of A.

  3. A is true but R is false.

  4. A is false but R is true.

  5. Both A and R are false.


Correct Option: B
Explanation:

This option is correct, because of steric hindrance between big sized Br-atoms, the energy difference between staggered and eclipsed forms of ethylene dibromide is more than that of ethylene dichloride.

Which of the following statements is/are true? A. The dihedral angle between the H-atom is staggered conformation of ethane is 60˚. B. C2H5O2N shows functional isomerism as well as tautomerism. C. Cyclopropane is better fuel than propane.

  1. Only A

  2. Only B

  3. A and C

  4. A, B and C

  5. None of these


Correct Option: D
Explanation:

This option is correct,  because dihedral angle between the H-atom is staggered conformation of ethane is 60˚, nitroethane shows tautomerism due to presence of α-hydrogens and functional isomerism with ethylnitrite and because of angle stain, the heat of combustion of cyclopropane is higher than that of propane.

Assertion: Stereoisomerisms which are not mirror images of each other are called diastereomers. Reason: Diastereomers may or may not be optically active.

  1. Both A and R are true and R is the correct explanation of A.

  2. Both A and R are true but R is NOT the correct explanation of A.

  3. A is true but R is false.

  4. A is false but R is true.

  5. Both A and R are false.


Correct Option: B
Explanation:

Since, diastereomers may or may not be chiral,  they may or may not be optically active. Thus, this option is correct.

Assertion: CHBr=CHCl exhibits geometrical isomerism but CH2Br-CH2Cl does not. Reason: Presence of C=C is one of the conditions of geometrical isomerism.

  1. Both A and R are true and R is the correct explanation of A.

  2. Both A and R are true but R is NOT the correct explanation of A.

  3. A is true but R is false.

  4. A is false but R is true.

  5. Both A and R are false.


Correct Option: C
Explanation:

CHBr=CHCl exhibits geometrical isomerism but CH2Br-CH2Cl does not, because the molecule may or may not contain a double bond, only restricted rotation about a bond give rise to geometrical isomerism. Thus, this option is correct.

Assertion: Benzaldehyde forms two oximes on reacting with NH2OH. Reason: The two oximes arise due to geometrical isomerism around C=N bond.

  1. Both A and R are true and R is the correct explanation of A.

  2. Both A and R are true but R is NOT the correct explanation of A.

  3. A is true but R is false.

  4. A is false but R is true.

  5. Both A and R are false.


Correct Option: A
Explanation:

Benzaldehyde forms two oximes on reacting with NH2OH because the two oximes arise due to geometrical isomerism around C=N bond. Thus, this option is correct.

Which of the following statements is/are false? A. Compounds containing one chiral carbon atom are always optically active. B. Maleic and fumeric acids are geometrical isomerism. C. Maleic acid is less soluble in water than fumeric acid.

  1. Only A

  2. Only B

  3. Only C

  4. A, B, and C

  5. None of these


Correct Option: C
Explanation:

This option is correct, because maleic acid being cis-isomer is less closely packed in the crystal lattice as compare to fumeric acid (trans-isomer), and hence is more soluble in water than fumeric acid.

Assertion: Propionic acid contains a prochiral carbon. Reason: Replacement of hydrogen atom of the CH2 group by Br-atom produces a chiral carbon.

  1. Both A and R are true and R is the correct explanation of A.

  2. Both A and R are true but R is NOT the correct explanation of A.

  3. A is true but R is false.

  4. A is false but R is true.

  5. Both A and R are false.


Correct Option: A
Explanation:

This option is correct, because propionic acid contains a prochiral carbon due to replacement of hydrogen atom of the CH2 group by Br-atom produces a chiral carbon.

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