TEST BANK for Organic Chemistry 6th Edition
h h h h h h
Smith / All Chapters 1 - 29 / Full Complete
h h h h h h h h h h
Page h1
,Chapter h1 hStructure hand hBonding
Chapter h2 hAcids hand hBases
Chapter h3 hIntroduction hto hOrganic hMolecules hand hFunctional hGroups
Chapter h4 hAlkanes
Chapter h5 hStereochemistry
Chapter h6 hUnderstanding hOrganic hReactions
Chapter h7 hAlkyl hHalides hand hNucleophilic hSubstitution
Chapter h8 hAlkyl hHalides hand hElimination hReactions
Chapter h9 hAlcohols, hEthers, hand hRelated hCompounds
Chapter h10 hAlkenes hand hAddition hReactions
Chapter h11 hAlkynes hand hSynthesis
Chapter h12 hOxidation hand hReduction
Spectroscopy hA hMass hSpectrometry
Spectroscopy hB hInfrared hSpectroscopy
Spectroscopy hC hNuclear hMagnetic hResonance hSpectroscopy
Chapter h13 hRadical hReactions
Chapter h14 hConjugation, hResonance, hand hDienes
Chapter h15 hBenzene hand hAromatic hCompounds
Chapter h16 hReactions hof hAromatic hCompounds
Chapter h17 hIntroduction hto hCarbonyl hChemistry: hOrganometallic hReagents;
hOxidation hand hReduction
Chapter h18 hAldehydes hand hKetones—Nucleophilic hAddition
Chapter h19 hCarboxylic hAcids hand hNitriles
Chapter h20 hCarboxylic hAcids hand hTheir hDerivatives- hNucleophilic hAcyl
hSubstitution
Chapter h21 hSubstitution hReactions hof hCarbonyl hCompounds hat hthe hα-Carbon
Chapter h22 hCarbonyl hCondensation hReactions
Chapter h23 hAmines
Chapter h24 hCarbon-Carbon hBond-Forming hReactions hin hOrganic hSynthesis
Chapter h25 hPericyclic hReactions
Chapter h26 hCarbohydrates
Chapter h27 hAmino hAcids hand hProteins
Chapter h28 hSynthetic hPolymers
Chapter h29 hLipids h(Available honline)
Page h2
, Chapter 1: Structure and Bonding
h h h h
1. What his hthe hground-state helectronic hconfiguration hof ha hcarbon
2 2 5
hatom? hA) h 1s , h2s , h2p B) h 1s2, h2s2, h2p2 C) h 1s2, h2s2,
6 2 2 4
h2p D) h 1s , h2s , h2p
2. What his hthe hground-state helectronic hconfiguration hof ha hfluorine
2 2 2
hatom?hA) h 1s , h2s , h2p B) h 1s2, h2s2, h2p3 C) h 1s2, h2s2,
4
h2p D) h 1s2, h2s2, h2p5
3. What his hthe hground-state helectronic hconfiguration hof ha hmagnesium hcation
2+
h(Mg )?hA) 1s2, h2s2, h2p6 C) 1s2, h2s2,
6 2
h2p , h3s
B) 1s2, h2s2, h2p6, h3s1 D) 1s2, h2s2, h2p6, h3s2, h3p2
4. What his hthe hground-state helectronic hconfiguration hof ha hchlorine hanion
—
h(Cl )?hA) 1s2, h2s2, h2p6 C)
1s2, h2s2, h2p6, h3s2, h3p5
B) 1s2, h2s2, h2p6, h3s2, h3p6 D) 1s2, h2s2, h2p6, h3s2, h3p4
5. Which hof hthe hfollowing hstatements habout hvalence helectrons his htrue?
A) They hare hthe hmost htightly hheld helectrons.
B) They hdo hnot hparticipate hin hchemical hreactions.
Page h3
, Chapter h1: hStructure hand
hBonding
C) They hare hthe houtermost helectrons.
D) They hreveal hthe hperiod hnumber hof ha hsecond-row helement.
6. Which hof hthe hfollowing hstatements habout hbonding his htrue?
A) Covalent hbonds hresult hfrom hthe htransfer hof helectrons hfrom hone helement hto hanother.
B) Ionic hbonds hresult hfrom hthe htransfer hof helectrons hfrom ha hmetal hto ha hnon-metal.
C) Ionic hbonds hresult hfrom hthe hsharing hof helectrons hbetween htwo hnon-metals.
D) Covalent hbonds hresult hfrom hthe hsharing hof helectrons hbetween htwo hmetals.
7. Which hof hthe hfollowing hwould hyou hexpect hto hhave hionic hbonds?
A) CO B) h FBr C) h NF3 D) h NaCl
8. Which hof hthe hfollowing hmolecules hhas hnonpolar hcovalent hbonds?
A) HCl B) h N2 C) h CHCl3 D) h NO
9. Which hof hthe hfollowing hmolecules hcontain hboth hcovalent hand hionic hbonds?
A) I, hII B) h I, hIV C) h II, hIII D) hII, hIV
10. Arrange hthe hfollowing hbonds hin hdecreasing horder hof hionic hcharacter, hputting hthe
hmosthionic hfirst.
A) I h> hII h> hIII h> hIV C) IV h> hIII h> hII h> hI
B) IV h> hII h> hI h> hIII D) IV h> hII h> hIII h> hI
11. Which hof hthe hfollowing hstatements hcorrectly hdescribes hthe htypical hnumber hof hbonds
hforhcarbon, hnitrogen, hand hoxygen hin hmost hneutral horganic hmolecules?
A) Carbon hforms h4 hcovalent hbonds, hnitrogen hforms h2 hcovalent hbonds hand hoxygen
hformsh3 hcovalent hbonds.
B) Carbon hforms h4 hcovalent hbonds, hnitrogen hforms h3 hcovalent hbonds hand hoxygen
hformsh2 hcovalent hbonds.
Page h4
h h h h h h
Smith / All Chapters 1 - 29 / Full Complete
h h h h h h h h h h
Page h1
,Chapter h1 hStructure hand hBonding
Chapter h2 hAcids hand hBases
Chapter h3 hIntroduction hto hOrganic hMolecules hand hFunctional hGroups
Chapter h4 hAlkanes
Chapter h5 hStereochemistry
Chapter h6 hUnderstanding hOrganic hReactions
Chapter h7 hAlkyl hHalides hand hNucleophilic hSubstitution
Chapter h8 hAlkyl hHalides hand hElimination hReactions
Chapter h9 hAlcohols, hEthers, hand hRelated hCompounds
Chapter h10 hAlkenes hand hAddition hReactions
Chapter h11 hAlkynes hand hSynthesis
Chapter h12 hOxidation hand hReduction
Spectroscopy hA hMass hSpectrometry
Spectroscopy hB hInfrared hSpectroscopy
Spectroscopy hC hNuclear hMagnetic hResonance hSpectroscopy
Chapter h13 hRadical hReactions
Chapter h14 hConjugation, hResonance, hand hDienes
Chapter h15 hBenzene hand hAromatic hCompounds
Chapter h16 hReactions hof hAromatic hCompounds
Chapter h17 hIntroduction hto hCarbonyl hChemistry: hOrganometallic hReagents;
hOxidation hand hReduction
Chapter h18 hAldehydes hand hKetones—Nucleophilic hAddition
Chapter h19 hCarboxylic hAcids hand hNitriles
Chapter h20 hCarboxylic hAcids hand hTheir hDerivatives- hNucleophilic hAcyl
hSubstitution
Chapter h21 hSubstitution hReactions hof hCarbonyl hCompounds hat hthe hα-Carbon
Chapter h22 hCarbonyl hCondensation hReactions
Chapter h23 hAmines
Chapter h24 hCarbon-Carbon hBond-Forming hReactions hin hOrganic hSynthesis
Chapter h25 hPericyclic hReactions
Chapter h26 hCarbohydrates
Chapter h27 hAmino hAcids hand hProteins
Chapter h28 hSynthetic hPolymers
Chapter h29 hLipids h(Available honline)
Page h2
, Chapter 1: Structure and Bonding
h h h h
1. What his hthe hground-state helectronic hconfiguration hof ha hcarbon
2 2 5
hatom? hA) h 1s , h2s , h2p B) h 1s2, h2s2, h2p2 C) h 1s2, h2s2,
6 2 2 4
h2p D) h 1s , h2s , h2p
2. What his hthe hground-state helectronic hconfiguration hof ha hfluorine
2 2 2
hatom?hA) h 1s , h2s , h2p B) h 1s2, h2s2, h2p3 C) h 1s2, h2s2,
4
h2p D) h 1s2, h2s2, h2p5
3. What his hthe hground-state helectronic hconfiguration hof ha hmagnesium hcation
2+
h(Mg )?hA) 1s2, h2s2, h2p6 C) 1s2, h2s2,
6 2
h2p , h3s
B) 1s2, h2s2, h2p6, h3s1 D) 1s2, h2s2, h2p6, h3s2, h3p2
4. What his hthe hground-state helectronic hconfiguration hof ha hchlorine hanion
—
h(Cl )?hA) 1s2, h2s2, h2p6 C)
1s2, h2s2, h2p6, h3s2, h3p5
B) 1s2, h2s2, h2p6, h3s2, h3p6 D) 1s2, h2s2, h2p6, h3s2, h3p4
5. Which hof hthe hfollowing hstatements habout hvalence helectrons his htrue?
A) They hare hthe hmost htightly hheld helectrons.
B) They hdo hnot hparticipate hin hchemical hreactions.
Page h3
, Chapter h1: hStructure hand
hBonding
C) They hare hthe houtermost helectrons.
D) They hreveal hthe hperiod hnumber hof ha hsecond-row helement.
6. Which hof hthe hfollowing hstatements habout hbonding his htrue?
A) Covalent hbonds hresult hfrom hthe htransfer hof helectrons hfrom hone helement hto hanother.
B) Ionic hbonds hresult hfrom hthe htransfer hof helectrons hfrom ha hmetal hto ha hnon-metal.
C) Ionic hbonds hresult hfrom hthe hsharing hof helectrons hbetween htwo hnon-metals.
D) Covalent hbonds hresult hfrom hthe hsharing hof helectrons hbetween htwo hmetals.
7. Which hof hthe hfollowing hwould hyou hexpect hto hhave hionic hbonds?
A) CO B) h FBr C) h NF3 D) h NaCl
8. Which hof hthe hfollowing hmolecules hhas hnonpolar hcovalent hbonds?
A) HCl B) h N2 C) h CHCl3 D) h NO
9. Which hof hthe hfollowing hmolecules hcontain hboth hcovalent hand hionic hbonds?
A) I, hII B) h I, hIV C) h II, hIII D) hII, hIV
10. Arrange hthe hfollowing hbonds hin hdecreasing horder hof hionic hcharacter, hputting hthe
hmosthionic hfirst.
A) I h> hII h> hIII h> hIV C) IV h> hIII h> hII h> hI
B) IV h> hII h> hI h> hIII D) IV h> hII h> hIII h> hI
11. Which hof hthe hfollowing hstatements hcorrectly hdescribes hthe htypical hnumber hof hbonds
hforhcarbon, hnitrogen, hand hoxygen hin hmost hneutral horganic hmolecules?
A) Carbon hforms h4 hcovalent hbonds, hnitrogen hforms h2 hcovalent hbonds hand hoxygen
hformsh3 hcovalent hbonds.
B) Carbon hforms h4 hcovalent hbonds, hnitrogen hforms h3 hcovalent hbonds hand hoxygen
hformsh2 hcovalent hbonds.
Page h4
