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 |