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TEST BANK for Organic Chemistry 6th Edition by Janice Smith. ISBN-. B) I = Chlorine; II = carbon; III = boron. D) I = Carbon; II = carbon; III = fluorine. 48. What is the nucleophilic site in the following compounds? A) I = Hydrogen; II =  electrons in bond; III = nitrogen. B) I = Oxygen; II = carbon; III = nitrogen. C) I = Hydrogen; II = carbon; III = carbon. Test Bank Page 37 TEST BANK for Organic Chemistry 6th Edition by Janice Smith. ISBN-. D) I = Oxygen; II =  electrons in bond; III = nitrogen. Chapter 3: Intro. to Organic Molecules & Functional Groups 1. Which of the following lists contains common heteroatoms found in organic molecules? A) N, O, S, P, Cl C) B) D) Na, Mg, O, N, Cl Na, O, S, P, Cl Na, Mg, S, N, Cl 2. Why do heteroatoms confer reactivity on a particular molecule? A) Because they have lone pairs and create electron-rich sites on carbon. B) Because they have lone pairs and create electron-deficient sites on carbon. C) Because they are electronegative and act as electrophiles. D) Because they are electropositive and act as nucleophiles. 3. Why do  bonds confer reactivity on a particular molecule? A) Because  bonds are difficult to break in chemical reactions. B) Because  bonds make a molecule an acid. C) Because  bonds are easily broken in chemical reactions. D) Because  bonds make a molecule an electrophile. 4. Which of the following molecules contain the same functional groups? Test Bank Page 38 TEST BANK

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TEST BANK for Organic Chemistry 6th Edition by Janice Smith. ISBN-. B) I = Chlorine; II = carbon; III = boron. D) I = Carbon; II = carbon; III = fluorine. 48. What is the nucleophilic site in the following compounds? A) I = Hydrogen; II =  electrons in bond; III = nitrogen. B) I = Oxygen; II = carbon; III = nitrogen. C) I = Hydrogen; II = carbon; III = carbon. Test Bank Page 37 TEST BANK for Organic Chemistry 6th Edition by Janice Smith. ISBN-. D) I = Oxygen; II =  electrons in bond; III = nitrogen. Chapter 3: Intro. to Organic Molecules & Functional Groups 1. Which of the following lists contains common heteroatoms found in organic molecules? A) N, O, S, P, Cl C) B) D) Na, Mg, O, N, Cl Na, O, S, P, Cl Na, Mg, S, N, Cl 2. Why do heteroatoms confer reactivity on a particular molecule? A) Because they have lone pairs and create electron-rich sites on carbon. B) Because they have lone pairs and create electron-deficient sites on carbon. C) Because they are electronegative and act as electrophiles. D) Because they are electropositive and act as nucleophiles. 3. Why do  bonds confer reactivity on a particular molecule? A) Because  bonds are difficult to break in chemical reactions. B) Because  bonds make a molecule an acid. C) Because  bonds are easily broken in chemical reactions. D) Because  bonds make a molecule an electrophile. 4. Which of the following molecules contain the same functional groups? Test Bank Page 38 TEST BANK

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TEST BANK for Organic Chemistry 6th Edition by Janice Smith. ISBN-. B) I = Chlorine; II = carbon; III = boron. D) I = Carbon; II = carbon; III = fluorine. 48. What is the nucleophilic site in the following compounds? A) I = Hydrogen; II = electrons in bond; III = nitrogen. B) I = Oxygen; II = carbon; III = nitrogen. C) I = Hydrogen; II = carbon; III = carbon. Test Bank Page 37 TEST BANK for Organic Chemistry 6th Edition by Janice Smith. ISBN-. D) I = Oxygen; II = electrons in bond; III = nitrogen. Chapter 3: Intro. to Organic Molecules & Functional Groups 1. Which of the following lists contains common heteroatoms found in organic molecules? A) N, O, S, P, Cl C) B) D) Na, Mg, O, N, Cl Na, O, S, P, Cl Na, Mg, S, N, Cl 2. Why do heteroatoms confer reactivity on a particular molecule? A) Because they have lone pairs and create electron-rich sites on carbon. B) Because they have lone pairs and create electron-deficient sites on carbon. C) Because they are electronegative and act as electro

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