Chapter c1 cStructure cand cBonding
cChapter c2 cAcids cand cBases
Chapter c3 cIntroduction cto cOrganic cMolecules cand cFunctional cGroups
cChapter c4 cAlkanes
Chapter c5 cStereochemistry
Chapter c6 cUnderstanding cOrganic cReactions
Chapter c7 cAlkyl cHalides cand cNucleophilic cSubstitution
cChapter c8 cAlkyl cHalides cand cElimination cReactions
cChapter c9 cAlcohols, cEthers, cand cRelated cCompounds
cChapter c10 cAlkenes cand cAddition cReactions
Chapter c11 cAlkynes cand cSynthesis
cChapter c12 cOxidation cand cReduction
cSpectroscopy cA cMass cSpectrometry
cSpectroscopy cB cInfrared cSpectroscopy
Spectroscopy cC cNuclear cMagnetic cResonance
cSpectroscopy cChapter c13 cRadical cReactions
Chapter c14 cConjugation, cResonance, cand cDienes
cChapter c15 cBenzene cand cAromatic cCompounds
cChapter c16 cReactions cof cAromatic cCompounds
Chapter c17 cIntroduction cto cCarbonyl cChemistry: cOrganometallic
cReagents; cOxidation cand cReduction
Chapter c18 cAldehydes cand cKetones—Nucleophilic
cAddition cChapter c19 cCarboxylic cAcids cand cNitriles
Chapter c20 cCarboxylic cAcids cand cTheir cDerivatives- cNucleophilic cAcyl
cSubstitution
Chapter c21 cSubstitution cReactions cof cCarbonyl cCompounds cat cthe cα-
Carbon cChapter c22 cCarbonyl cCondensation cReactions
Chapter c23 cAmines
Chapter c24 cCarbon-Carbon cBond-Forming cReactions cin cOrganic cSynthesis
Page c2
,cChapter c25 cPericyclic cReactions
Chapter c26 cCarbohydrates
Chapter c27 cAmino cAcids cand cProteins
cChapter c28 cSynthetic cPolymers
cChapter c29 cLipids c(Available conline)
Page c3
, Chapter c1: cStructure cand cBonding
1. What c is cthe cground-state celectronic cconfiguration cof ca ccarbon catom?
A) 1s2, c2s2, c2p5 B) c 1s2, c2s2, c2p2 C) c 1s2, c2s2, c2p6 D) c 1s2, c2s2, c2p4
2. What c is cthe cground-state celectronic cconfiguration cof ca cfluorine catom?
A) 1s2, c2s2, c2p2 B) c 1s2, c2s2, c2p3 C) c 1s2, c2s2, c2p4 D) c 1s2, c2s2, c2p5
3. What cis cthe cground-state celectronic cconfiguration cof ca cmagnesium ccation c(Mg2+)?
A) 1s2, c2s2, c2p6 C) 1s2, c2s2, c2p6, c3s2
B) 1s2, c2s2, c2p6, c3s1 D) 1s2, c2s2, c2p6, c3s2, c3p2
4. What cis cthe cground-state celectronic cconfiguration cof ca cchlorine canion c(Cl—)?
A) 1s2, c2s2, c2p6 C) 1s2, c2s2, c2p6, c3s2, c3p5
B) 1s2, c2s2, c2p6, c3s2, c3p6 D) 1s2, c2s2, c2p6, c3s2, c3p4
5. Which cof cthe cfollowing cstatements cabout cvalence celectrons cis ctrue?
A) They care cthe cmost ctightly cheld celectrons.
B) They cdo cnot cparticipate cin cchemical creactions.
Page c4
, Chapter c1: cStructure cand
cBonding
C) They care cthe coutermost celectrons.
D) They creveal cthe cperiod cnumber cof ca csecond-row celement.
6. Which cof cthe cfollowing cstatements cabout cbonding cis ctrue?
A) Covalent cbonds cresult c from cthe ctransfer cof celectrons cfrom cone celement cto
c another.
B) Ionic cbonds cresult c from cthe ctransfer cof celectrons cfrom ca cmetal cto ca cnon-metal.
C) Ionic cbonds cresult cfrom cthe csharing cof celectrons cbetween ctwo cnon-metals.
D) Covalent cbonds cresult c from cthe csharing cof celectrons cbetween ctwo cmetals.
7. Which cof cthe cfollowing cwould cyou cexpect cto chave cionic cbonds?
A) CO B) c FBr C) c NF3 D) c NaCl
8. Which cof cthe cfollowing cmolecules chas cnonpolar ccovalent cbonds?
A) HCl B) c N2 C) c CHCl3 D) c NO
9. Which cof cthe cfollowing cmolecules ccontain cboth ccovalent cand cionic cbonds?
A) I, cII B) c I, cIV C) c II, cIII D) cII, cIV
10. Arrange cthe cfollowing cbonds cin cdecreasing corder cof cionic ccharacter, cputting cthe
cmost cionic cfirst.
A) I c > cII c> cIII c> cIV C) IV c> cIII c> cII c> cI
B) IV c> cII c> cI c> cIII D) IV c> cII c> cIII c> cI
11. Which cof cthe cfollowing cstatements ccorrectly cdescribes cthe ctypical cnumber cof
cbonds cfor ccarbon, cnitrogen, cand coxygen cin cmost cneutral corganic cmolecules?
A) Carbon cforms c4 ccovalent cbonds, cnitrogen cforms c2 ccovalent cbonds cand coxygen
cforms c3 ccovalent cbonds.
B) Carbon cforms c4 ccovalent cbonds, cnitrogen cforms c3 ccovalent cbonds cand coxygen
cforms c2 ccovalent cbonds.
Page c5
cChapter c2 cAcids cand cBases
Chapter c3 cIntroduction cto cOrganic cMolecules cand cFunctional cGroups
cChapter c4 cAlkanes
Chapter c5 cStereochemistry
Chapter c6 cUnderstanding cOrganic cReactions
Chapter c7 cAlkyl cHalides cand cNucleophilic cSubstitution
cChapter c8 cAlkyl cHalides cand cElimination cReactions
cChapter c9 cAlcohols, cEthers, cand cRelated cCompounds
cChapter c10 cAlkenes cand cAddition cReactions
Chapter c11 cAlkynes cand cSynthesis
cChapter c12 cOxidation cand cReduction
cSpectroscopy cA cMass cSpectrometry
cSpectroscopy cB cInfrared cSpectroscopy
Spectroscopy cC cNuclear cMagnetic cResonance
cSpectroscopy cChapter c13 cRadical cReactions
Chapter c14 cConjugation, cResonance, cand cDienes
cChapter c15 cBenzene cand cAromatic cCompounds
cChapter c16 cReactions cof cAromatic cCompounds
Chapter c17 cIntroduction cto cCarbonyl cChemistry: cOrganometallic
cReagents; cOxidation cand cReduction
Chapter c18 cAldehydes cand cKetones—Nucleophilic
cAddition cChapter c19 cCarboxylic cAcids cand cNitriles
Chapter c20 cCarboxylic cAcids cand cTheir cDerivatives- cNucleophilic cAcyl
cSubstitution
Chapter c21 cSubstitution cReactions cof cCarbonyl cCompounds cat cthe cα-
Carbon cChapter c22 cCarbonyl cCondensation cReactions
Chapter c23 cAmines
Chapter c24 cCarbon-Carbon cBond-Forming cReactions cin cOrganic cSynthesis
Page c2
,cChapter c25 cPericyclic cReactions
Chapter c26 cCarbohydrates
Chapter c27 cAmino cAcids cand cProteins
cChapter c28 cSynthetic cPolymers
cChapter c29 cLipids c(Available conline)
Page c3
, Chapter c1: cStructure cand cBonding
1. What c is cthe cground-state celectronic cconfiguration cof ca ccarbon catom?
A) 1s2, c2s2, c2p5 B) c 1s2, c2s2, c2p2 C) c 1s2, c2s2, c2p6 D) c 1s2, c2s2, c2p4
2. What c is cthe cground-state celectronic cconfiguration cof ca cfluorine catom?
A) 1s2, c2s2, c2p2 B) c 1s2, c2s2, c2p3 C) c 1s2, c2s2, c2p4 D) c 1s2, c2s2, c2p5
3. What cis cthe cground-state celectronic cconfiguration cof ca cmagnesium ccation c(Mg2+)?
A) 1s2, c2s2, c2p6 C) 1s2, c2s2, c2p6, c3s2
B) 1s2, c2s2, c2p6, c3s1 D) 1s2, c2s2, c2p6, c3s2, c3p2
4. What cis cthe cground-state celectronic cconfiguration cof ca cchlorine canion c(Cl—)?
A) 1s2, c2s2, c2p6 C) 1s2, c2s2, c2p6, c3s2, c3p5
B) 1s2, c2s2, c2p6, c3s2, c3p6 D) 1s2, c2s2, c2p6, c3s2, c3p4
5. Which cof cthe cfollowing cstatements cabout cvalence celectrons cis ctrue?
A) They care cthe cmost ctightly cheld celectrons.
B) They cdo cnot cparticipate cin cchemical creactions.
Page c4
, Chapter c1: cStructure cand
cBonding
C) They care cthe coutermost celectrons.
D) They creveal cthe cperiod cnumber cof ca csecond-row celement.
6. Which cof cthe cfollowing cstatements cabout cbonding cis ctrue?
A) Covalent cbonds cresult c from cthe ctransfer cof celectrons cfrom cone celement cto
c another.
B) Ionic cbonds cresult c from cthe ctransfer cof celectrons cfrom ca cmetal cto ca cnon-metal.
C) Ionic cbonds cresult cfrom cthe csharing cof celectrons cbetween ctwo cnon-metals.
D) Covalent cbonds cresult c from cthe csharing cof celectrons cbetween ctwo cmetals.
7. Which cof cthe cfollowing cwould cyou cexpect cto chave cionic cbonds?
A) CO B) c FBr C) c NF3 D) c NaCl
8. Which cof cthe cfollowing cmolecules chas cnonpolar ccovalent cbonds?
A) HCl B) c N2 C) c CHCl3 D) c NO
9. Which cof cthe cfollowing cmolecules ccontain cboth ccovalent cand cionic cbonds?
A) I, cII B) c I, cIV C) c II, cIII D) cII, cIV
10. Arrange cthe cfollowing cbonds cin cdecreasing corder cof cionic ccharacter, cputting cthe
cmost cionic cfirst.
A) I c > cII c> cIII c> cIV C) IV c> cIII c> cII c> cI
B) IV c> cII c> cI c> cIII D) IV c> cII c> cIII c> cI
11. Which cof cthe cfollowing cstatements ccorrectly cdescribes cthe ctypical cnumber cof
cbonds cfor ccarbon, cnitrogen, cand coxygen cin cmost cneutral corganic cmolecules?
A) Carbon cforms c4 ccovalent cbonds, cnitrogen cforms c2 ccovalent cbonds cand coxygen
cforms c3 ccovalent cbonds.
B) Carbon cforms c4 ccovalent cbonds, cnitrogen cforms c3 ccovalent cbonds cand coxygen
cforms c2 ccovalent cbonds.
Page c5
