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Test BANK Organic Chemistry 6th Edition by Janice Gorzynski Smith | Verified Chapters 1 - 29

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Test BANK for Organic Chemistry 6th Edition by Janice Gorzynski Smith Stuvia Is Available For Download After Purchase. In Case You Encounter Any Difficulties with Download or want the document in a Different Format, Please Feel Free to Contact Me via Inbox. I Will Promptly Sort You. Thank You Test BANK for Organic Chemistry 6th Edition by Janice Gorzynski Smith is a valuable study resource designed to help you grasp complex organic chemistry concepts with ease. Whether you’re preparing for exams or need extra practice, this test bank provides a wide range of exam questions that reinforce key topics and improve your problem-solving skills. With the Organic Chemistry 6th Edition Test Bank, you can deepen your understanding of reaction mechanisms, molecular structures, and synthesis strategies. It serves as an excellent companion to your textbook, allowing you to test your knowledge and build confidence. If you’re using the Janice Smith Organic Chemistry Test Bank, you’ll find it helpful for reviewing essential principles and mastering challenging concepts. Ideal for chemistry students at all levels, this test bank for chemistry students offers a reliable way to enhance your study sessions. Download the Chemistry 6th Edition Test Bank to access practice questions that will strengthen your grasp of organic chemistry and improve your performance in exams. Here is your cleaned-up text with the unintended "v" characters removed while keeping everything else the same: --- 1. What is the ground-state electronic configuration of a carbon atom? A) 1s² 2s² 2p⁵ B) 1s² 2s² 2p² C) 1s² 2s² 2p⁶ D) 1s² 2s² 2p⁴ 2. What is the ground-state electronic configuration of a fluorine atom? A) 1s² 2s² 2p² B) 1s² 2s² 2p³ C) 1s² 2s² 2p⁴ D) 1s² 2s² 2p⁵ 3. What is the ground-state electronic configuration of a magnesium cation (Mg²⁺)? A) 1s² 2s² 2p⁶ B) 1s² 2s² 2p⁶ 3s¹ C) 1s² 2s² 2p⁶ 3s² D) 1s² 2s² 2p⁶ 3s² 3p² 4. What is the ground-state electronic configuration of a chlorine anion (Cl⁻)? A) 1s² 2s² 2p⁶ B) 1s² 2s² 2p⁶ 3s² 3p⁶ C) 1s² 2s² 2p⁶ 3s² 3p⁵ D) 1s² 2s² 2p⁶ 3s² 3p⁴ 5. Which of the following statements about valence electrons is true? A) They are the most tightly held electrons. B) They do not participate in chemical reactions. C) They are the outermost electrons. D) They reveal the period number of a second-row element. 6. Which of the following statements about bonding is true? A) Covalent bonds result from the transfer of electrons from one element to another. B) Ionic bonds result from the transfer of electrons from a metal to a non-metal. C) Ionic bonds result from the sharing of electrons between two non-metals. D) Covalent bonds result from the sharing of electrons between two metals. 7. Which of the following would you expect to have ionic bonds? A) CO B) FBr C) NF₃ D) NaCl 8. Which of the following molecules has nonpolar covalent bonds? A) HCl B) N₂ C) CHCl₃ D) NO 9. Which of the following molecules contain both covalent and ionic bonds? A) I, II B) I, IV C) II, III D) II, IV 10. Arrange the following bonds in decreasing order of ionic character, putting the most ionic first. A) I > II > III > IV B) IV > II > I > III C) IV > III > II > I D) IV > II > III > I 11. Which of the following statements correctly describes the typical number of bonds for carbon, nitrogen, and oxygen in most neutral organic molecules? A) Carbon forms 4 covalent bonds, nitrogen forms 2 covalent bonds, and oxygen forms 3 covalent bonds. B) Carbon forms 4 covalent bonds, nitrogen forms 3 covalent bonds, and oxygen forms 2 covalent bonds. C) Carbon forms 4 covalent bonds, nitrogen forms 5 covalent bonds, and oxygen forms 2 covalent bonds. D) Carbon forms 4 covalent bonds, nitrogen forms 5 covalent bonds, and oxygen forms 4 covalent bonds. 12. Which is not an acceptable Lewis structure for the anion CH₂NCO⁻? A) I B) II C) III D) IV 13. Which of the following Lewis structures is correct? A) I B) II C) III D) IV 14. Which of the following Lewis structures is correct? A) I, II B) I, III C) II, III D) III, IV 15. Which is the correct Lewis structure for acetic acid (CH₃CO₂H)?

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Organic Chemistry 6th Edition By Smith
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Organic Chemistry 6th Edition by Smith











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Institution
Organic Chemistry 6th Edition by Smith
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Organic Chemistry 6th Edition by Smith

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Uploaded on
February 8, 2025
Number of pages
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Written in
2024/2025
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TEST BANK
Organic Chemistry 6th Edition By Smith
All Chapters 1 - 29




Pagev1

,Chapterv1vStructurevandvBonding
Chapterv2vAcidsvandvBases
Chapterv3vIntroductionvtovOrganicvMoleculesvandvFunctionalvGroups
Chapterv4vAlkanes
Chapterv5vStereochemistry
Chapterv6vUnderstandingvOrganicvReactions
Chapterv7vAlkylvHalidesvandvNucleophilicvSubstitution
Chapterv8vAlkylvHalidesvandvEliminationvReactions
Chapterv9vAlcohols,vEthers,vandvRelatedvCompounds
Chapterv10vAlkenesvandvAdditionvReactions
Chapterv11vAlkynesvandvSynthesis
Chapterv12vOxidationvandvReduction
SpectroscopyvAvMassvSpectrometry
SpectroscopyvBvInfraredvSpectroscopy
SpectroscopyvCvNuclearvMagneticvResonancevSpectroscopy
Chapterv13vRadicalvReactions
Chapterv14vConjugation,vResonance,vandvDienes
Chapterv15vBenzenevandvAromaticvCompounds
Chapterv16vReactionsvofvAromaticvCompounds
Chapterv17vIntroductionvtovCarbonylvChemistry:vOrganometallicvReagents;vOxid
ationvandvReduction
Chapterv18vAldehydesvandvKetones—NucleophilicvAddition
Chapterv19vCarboxylicvAcidsvandvNitriles
Chapterv20vCarboxylicvAcidsvandvTheirvDerivatives-
vNucleophilicvAcylvSubstitution




Chapterv21vSubstitutionvReactionsvofvCarbonylvCompoundsvatvthevα-Carbon
Chapterv22vCarbonylvCondensationvReactions
Chapterv23vAmines
Chapterv24vCarbon-CarbonvBond-FormingvReactionsvinvOrganicvSynthesis
Chapterv25vPericyclicvReactions
Chapterv26vCarbohydrates
Chapterv27vAminovAcidsvandvProteins
Chapterv28vSyntheticvPolymers
Chapterv29vLipidsv(Availablevonline)

Pagev2

, Chapter 1: Structure and Bonding
v v v v




1. Whatvisvthevground-
statevelectronicvconfigurationvofvavcarbonvatom?vA)v 1s2,v2s2,v2p5
B)v 1s2,v2s2,v2p2 C)v 1s2,v2s2,v2p6 D)v 1s2,v2s2,v2p4

2. Whatvisvthevground-
statevelectronicvconfigurationvofvavfluorinevatom?vA)v 1s2,v2s2,v2p2
B)v 1s2,v2s2,v2p3 C)v 1s2,v2s2,v2p4 D)v 1s2,v2s2,v2p5

3. Whatvisvthevground-
statevelectronicvconfigurationvofvavmagnesiumvcationv(Mg2+)?vA) 1s2,v2s2,v2p6
C) 1s2,v2s2,v2p6,v3s2
B) 1s2,v2s2,v2p6,v3s1 D) 1s2,v2s2,v2p6,v3s2,v3p2


4. Whatvisvthevground-statevelectronicvconfigurationvofvavchlorinevanionv(Cl—
)?vA) 1s2,v2s2,v2p6 C) 1s2,v2s2,v2p6,v3s2,v3p5
B) 1s2,v2s2,v2p6,v3s2,v3p6 D) 1s2,v2s2,v2p6,v3s2,v3p4


5. Whichvofvthevfollowingvstatementsvaboutvvalencevelectronsvisvtrue?
A) Theyvarevthevmostvtightlyvheldvelectrons.
B) Theyvdovnotvparticipatevinvchemicalvreactions.




Pagev3

, Chapterv1:vStructurevandvBondin
g

C) Theyvarevthevoutermostvelectrons.
D) Theyvrevealvthevperiodvnumbervofvavsecond-rowvelement.


6. Whichvofvthevfollowingvstatementsvaboutvbondingvisvtrue?
A) Covalentvbondsvresultvfromvthevtransfervofvelectronsvfromvonevelementvtovanother.
B) Ionicvbondsvresultvfromvthevtransfervofvelectronsvfromvavmetalvtovavnon-metal.
C) Ionicvbondsvresultvfromvthevsharingvofvelectronsvbetweenvtwovnon-metals.
D) Covalentvbondsvresultvfromvthevsharingvofvelectronsvbetweenvtwovmetals.


7. Whichvofvthevfollowingvwouldvyouvexpectvtovhavevionicvbonds?
A) CO B)v FBr C)v NF3 D)v NaCl



8. Whichvofvthevfollowingvmoleculesvhasvnonpolarvcovalentvbonds?
A) HCl B)v N2 C)v CHCl3 D)v NO

9. Whichvofvthevfollowingvmoleculesvcontainvbothvcovalentvandvionicvbonds?




A) I,vII B)v I,vIV C)v II,vIII D)vII,vIV

10. Arrangevthevfollowingvbondsvinvdecreasingvordervofvionicvcharacter,vputtingvthevmostv
ionicvfirst.




A) Iv>vIIv>vIIIv>vIV C) IVv>vIIIv>vIIv>vI
B) IVv>vIIv>vIv>vIII D) IVv>vIIv>vIIIv>vI


11. Whichvofvthevfollowingvstatementsvcorrectlyvdescribesvthevtypicalvnumbervofvbondsvforv
carbon,vnitrogen,vandvoxygenvinvmostvneutralvorganicvmolecules?
A) Carbonvformsv4vcovalentvbonds,vnitrogenvformsv2vcovalentvbondsvandvoxygenvformsv
3vcovalentvbonds.
B) Carbonvformsv4vcovalentvbonds,vnitrogenvformsv3vcovalentvbondsvandvoxygenvformsv
2vcovalentvbonds.




Pagev4

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