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ACADEMICS

CHM 202 Quiz – Covalent Bond and Organic Reactions

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Created on By Oluwaferanmi Akinyele

CHM 202 Quiz - Covalent Bond and Organic Reactions

This CHM 202 Quiz is based on the first slide - Covalent Bond and Organic Reactions.

It covers topics including covalent bonds, intermolecular forces, factors affecting organic reactions (Inductive effect, Mesomeric effect, Resonance effect, Steric effect), and types of organic reactions....etc

This quiz contains 25 multiple choice questions for 20 mins, gotten from last year's exam questions, Wade textbook, and other sources.

Best of luck.

1 / 25

Which intermolecular force is the weakest and often disappears and reappears due to the movement of atoms?

2 / 25

What type of solvent can solvate both cations and anions?

3 / 25

Which of the following is a polar aprotic solvent?

4 / 25

How many chiral carbons do glucose and fructose each have?

5 / 25

Which notation is used to designate the spatial arrangement of atoms in an optically active compound?

6 / 25

Which of the following represents the product of the SN2 reaction between CH3CH2ONa and CH3CH2Cl?

7 / 25

How many optical isomers does a compound with two chiral carbon atoms possess?

8 / 25

Which of the following molecules exhibits hydrogen bonding?

9 / 25

In a nucleophilic substitution reaction, the nucleophile is a:

10 / 25

Arrange the following in order of decreasing boiling point: HF; H2O; Hal

11 / 25

The boiling point of a substance increases with the strength of the intermolecular forces between its molecules. Which of the following substances would be expected to have the highest boiling point?

12 / 25

Arrange the following in decreasing order of acidity; Ethnic acid; dichloroethanoic acid; monochloroethanoic acid; and trichloroethanoic acid. Give reason for your answer.

13 / 25

What is the product of the heterolytic cleavage of a covalent bond?

14 / 25

Which of the following compounds undergoes racemization?

15 / 25

Alkanes can be prepared by the following methods except; (i) Dehydrohalogenation (ii) Hydration of alkenes (iii) Hydrogenation of unsaturated hydrocarbons (iv) Electrophilic addition reaction.

16 / 25

What is the IUPAC name of the following compound: CH3CH2CH(CH3)CH2CH3?

17 / 25

Give the total number of resonance canonical structures for methoxybenzene and the number of the canonical structures that are ionic;

18 / 25

How many chiral centre(s) are there in 1-bromo-1,2-dihydroxylpropane?

19 / 25

Which of the following statements about resonance is true?

20 / 25

The following is/are correct for SN1 reaction mechanism except; (i) The geometry of the transition state (ii) It is favoured with primary alkyl halide (iii) The substrate and product are of opposite configuration (iv) The product are of the same geometry

21 / 25

In the Lewis structure of methanol (CH3OH), how many lone pairs of electrons are present on the oxygen atom?

22 / 25

In an SN1 reaction between a tertiary alkyl halide and water, the rate-determining step involves:

23 / 25

Why does NaCl dissolve readily in water but not in benzene?

24 / 25

Consider the above compound: How many chiral C-atoms are present; Indicate the specific configuartion of all C-atoms present and give the number of optically active isomers of the compound.

 

 

25 / 25

Which alkyl halides(s) would undergo dehydrogenation to give the following pure alkene, methylenecyclohexane?

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