| A. sp, sp3 and sp2, respectively | ||
| B. sp3, sp2, and sp, respectively | ||
| C. sp2, sp, and sp3, respectively | ||
| D. sp, sp, and sp2, respectively |
| A. Linear, tetrahedral, and planar, respectively | ||
| B. Tetrahedral, Linear, and planar, respectively | ||
| C. Linear, Linear, and planar, respectively | ||
| D. Tetrahedral, planar, and linear, respectively |
| A. +1, -1 | ||
| B. +1, +1 | ||
| C. -1, -1 | ||
| D. -1, +1 |
| A. Van der Waals attraction | ||
| B. Hydrogen bonding | ||
| C. Ionic bonding | ||
| D. Covalent bonding |
Fill in the blank. The strongest type of intermolecular force occurring between neutral molecules is the __________________.
| A. Covalent bond | ||
| B. Ionic bond | ||
| C. Van der Waals force | ||
| D. Hydrogen bond |
When the products of a chemical reaction are more stable energetically than the reactants, energy is released as heat. This type of reaction
is referred to as which of the following?
| A. Exothermic | ||
| B. Endothermic | ||
| C. Analgesic | ||
| D. Endodermic |
Fill in the blank. A high energy transition state must be reached for chemical bonds to be broken and products formed in a chemical reaction.
The amount of energy needed to reach this transition state is known as the _________________.
| A. Trans energy | ||
| B. Static energic | ||
| C. Kinetic energy | ||
| D. Activation energy |
Fill in the blank. In an acid-base reaction, proton donors are __________________.
| A. Bronsted acids | ||
| B. Lowry Bases | ||
| C. Bronsted-Lowry Acids | ||
| D. Bronsted-Lowry Bases |
| A. Anion effect | ||
| B. Cation effect | ||
| C. Hydrogen effect | ||
| D. Hydroxide effect |
In a chemical reaction, what is the species that supplies a pair of electrons to form a covalent bond called?
| A. Lewis acid | ||
| B. Hydrogen species | ||
| C. Lewis protons | ||
| D. Lewis base |
The molecular formula CnH2n-2 is the general formula for which group of hydrocarbons?
| A. Alkanes | ||
| B. Alkenes | ||
| C. Cycloalkanes | ||
| D. Alkynes |
The prefixes eth-, but-, hex-, and hept, represent hydrocarbon chains having how many carbon atoms?
| A. 2, 4, 6, 7, respectively | ||
| B. 2, 6, 4, 7, respectively | ||
| C. 4, 2, 7, 6, respectively | ||
| D. 2, 7, 6, 4, respectively |
In which reaction type does the number of σ-bonds in the substrate decrease as new π-bonds are formed?
| A. Elimination | ||
| B. Substitution | ||
| C. Addition | ||
| D. Combustion |
In the which of the following reaction types does the number of σ-bonds in the substrate molecule increase? In addition, in this reaction type, one or more π-bonds are usually lost.
| A. Elimination | ||
| B. Addition | ||
| C. Substitution | ||
| D. Combusion |
Which type of reaction is characterized by replacement of an atom or group by another; in this reaction type, the number of bonds does not change except for the added groups?
.
| A. Elimination | ||
| B. Addition | ||
| C. Substitution | ||
| D. Free radical |
| A. A free radical | ||
| B. A carbocation | ||
| C. An isotope | ||
| D. An isomer |
Carbon radicals are characterized by a lone electron on the carbon atom and have a total of how many valence electrons?
| A. Seven | ||
| B. Four | ||
| C. Eight | ||
| D. One |
Electrophiles are attracted to which of the following molecules?
| A. Both NH3 and NH4+ | ||
| B. Both CH3 O- and NH3 | ||
| C. Both CH3O- and K + | ||
| D. NH3, NH4+, CH3O-, and K + |
Nucleophiles are electron rich species or groups. Which of the following is an example of a nucleophile?
| A. NH4+ | ||
| B. H3O+ | ||
| C. NH3 | ||
| D. CH3OH |
| A. An electron | ||
| B. A free radical | ||
| C. A neutron | ||
| D. A proton |
Which of the followingis the correct line formula for3-methylpentane?
Which of the followingis the correct line formula for tert-butylcyclopentane?
WWhich of the followingis the correct formula for 3-ethyl-5-methyloctane?
The stereoisomer trans-1,3-dimethylcyclopentane is represented by which of the following structures?
In which of the following cyclohexane structures is a Cl group cis to a methyl group?
| A. The staggered conformation is the most stable. | ||
| B. The eclipsed form is the most stable. | ||
| C. The staggered and the eclipsed form have the same energy. | ||
| D. There are three stable staggered forms and two unstable eclipsed forms. |
| A. Cl, F, Br, I | ||
| B. Cl, Br, I, F | ||
| C. F, Cl, Br, I | ||
| D. I, Br, Cl, F |
| A. Anti | ||
| B. Gauche | ||
| C. Eclipsed | ||
| D. Fully eclipsed |
| A. 2 CO2+ 2H2O + heat | ||
| B. CO2+ 2H2O + heat | ||
| C. 2 CO2+ 3H2O + heat | ||
| D. CO2+ 3H2O + heat |
| A. Give a substitution product when the cation bonds to a nucleophile | ||
| B. Give an alkene product when the cation transfers a beta-proton to a base | ||
| C. Produce a substitution or an elimination after carbocation rearrangement | ||
| D. All of the above |
| A. Primary alkyl halides | ||
| B. Nonpolar aprotic solvent | ||
| C. Tertiary alkyl halides | ||
| D. Less substituted alkyl halides |
| A. SN3 | ||
| B. SN1 | ||
| C. SN2 | ||
| D. E2 |
| A. First order | ||
| B. Zero order | ||
| C. Third order | ||
| D. One half order |
| A. Constitutional isomers | ||
| B. Stereoisomers | ||
| C. Tautomers | ||
| D. Stable structural isomers |
| A. Diastereomers | ||
| B. Meso compounds | ||
| C. Enantiomers | ||
| D. A racemic mixture |
| A. Meso compounds | ||
| B. Racemates | ||
| C. Diastereoisomers | ||
| D. Chiral centers |
| A. Enantiomers | ||
| B. Diastereoisomers | ||
| C. Meso compounds | ||
| D. Racemates |
| A. Chiral compound | ||
| B. Achiral compound | ||
| C. Racemic mixture | ||
| D. Meso compound |
| A. An achiral mixture | ||
| B. A stereoisomeric mixture | ||
| C. A meso compound | ||
| D. A racemate |
| A. Racemates are not optically active. | ||
| B. Individual enantiomers are not optically active. | ||
| C. Achiral compounds are not optically active. | ||
| D. Meso compounds are not optically active. |
| A. CH3SH + NaBr | ||
| B. CH3SH only | ||
| C. CH3OH + NaBr | ||
| D. NaBr only |
| A. Because they are basic and nucleophilic | ||
| B. Because they are basic and electrophilic | ||
| C. Because they are acidic and electrophilic | ||
| D. Because they are positively charged |
Why are alcohols are much stronger acids than alkanes?
| A. Because both carbon and hydrogen are electrophilic in alcohols | ||
| B. Because the electronegativity of oxygen is substantially greater than that of carbon and hydrogen | ||
| C. Because the covalent bonds of the alcohol functional group are polarized | ||
| D. All of the above |
| A. Two pi bonds | ||
| B. One sigma and two pi bonds | ||
| C. Two sigma bonds | ||
| D. One sigma and one pi bond |
| A. One ring and one double bond. | ||
| B. Two rings and one double bond. | ||
| C. Two rings. | ||
| D. One triple bond. |
| A. Because alkenes have pi bonds | ||
| B. Because of hyperconjugation | ||
| C. Because of steric hindrance | ||
| D. Because cis isomers typically do not react in reactions |
| A. Propagation | ||
| B. Initiation | ||
| C. Bromine preparation | ||
| D. Termination |
| A. The reaction is a one-step reaction. | ||
| B. The geometry of the reaction is syn. | ||
| C. It occurs via a carbocation intermediate. | ||
| D. It takes place with a retention of configuration. |
| A. Solids and liquids | ||
| B. Liquids and gases | ||
| C. Solids and gases | ||
| D. Solids, liquids, and gases |
| A. sp2 hybridation of the carbons | ||
| B. sp3 hybridation of the carbons | ||
| C. sp hybridation of the carbons | ||
| D. sp3 d hybridation of the carbons |
| A. The nonpolar bonding strength | ||
| B. The linear geometry | ||
| C. Acidity | ||
| D. All of the above |