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Tor A Benzonitrile Styrene Toluene Xylene D A15. The mechanism of halogenation, nitration, sulfonation, alkylation and acylation of aromatic rings are best described as: A Nucleophilic Aliphatic Substitution Electrophilic Aromatic Substitution Electrophilic Aromatic Addition |Nucleophilic Aromatic Addition B D A16. Below is a table depicting two examples of nucleophiles capable of partaking in addition reactions with carbonyl groups. Complete Table 1, below, by assigning 1-4. Table 1: Nucleophiles for addition reactions to carbonyl groups. Name Water alcohol Reagent H20 Nu-H Nu 3 ROH 4 | 1 = HO-OH; 2 = H ; 3 = RO-H; 4 = HO- 1= HO-H; 2 = H"; 3 = RO-H; 4 = HO" C 1= HO-H; 2 = OH"; 3 = RO-R; 4 = HO- D A В 1 = HO-H; 2 = OH"; 3 = RO-H; 4 = RO- A17. Which of the following is the correct IUPAC name for the molecule below? CH, он | 6-methylheptanoic acid 6-methylhexanoic acid 6-dimethylhexanoic acid D A 6-methyloctanoic acid

Tor A Benzonitrile Styrene Toluene Xylene D A15. The mechanism of halogenation, nitration, sulfonation, alkylation and acylation of aromatic rings are best described as: A Nucleophilic Aliphatic Substitution Electrophilic Aromatic Substitution Electrophilic Aromatic Addition |Nucleophilic Aromatic Addition B D A16. Below is a table depicting two examples of nucleophiles capable of partaking in addition reactions with carbonyl groups. Complete Table 1, below, by assigning 1-4. Table 1: Nucleophiles for addition reactions to carbonyl groups. Name Water alcohol Reagent H20 Nu-H Nu 3 ROH 4 | 1 = HO-OH; 2 = H ; 3 = RO-H; 4 = HO- 1= HO-H; 2 = H"; 3 = RO-H; 4 = HO" C 1= HO-H; 2 = OH"; 3 = RO-R; 4 = HO- D A В 1 = HO-H; 2 = OH"; 3 = RO-H; 4 = RO- A17. Which of the following is the correct IUPAC name for the molecule below? CH, он | 6-methylheptanoic acid 6-methylhexanoic acid 6-dimethylhexanoic acid D A 6-methyloctanoic acid

Chemistry
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Page < 5 > of 11 ZOOM + Section A (continued) A14. What is the common name for methylbenzene? Benzonitrile Styrene Toluene Xylene A15. The mechanism of halogenation, nitration, sulfonation, alkylation and acylation of aromatic rings are best described as: Nucleophilic Aliphatic Substitution В A Electrophilic Aromatic Substitution Electrophilic Aromatic Addition Nucleophilic Aromatic Addition A16. Below is a table depicting two examples of nucleophiles capable of partaking in addition reactions with carbonyl groups. Complete Table 1, below, by assigning 1-4. Table 1: Nucleophiles for addition reactions to carbonyl groups. Name Nu-H Reagent H2O ROH Nu- 1 Water alcohol 1 = HO-OH; 2 =H¯; 3 = RO-H; 4 = HO- В A %3D 1 = HO-H; 2 = H¯; 3 = RO-H; 4 = HO 1 = HO-H; 2 = OH-; 3 = RO-R; 4 = HO- 1 %3D НО-Н; 2 - ОН;3 — RO-H; 4 %3D RO- %3D A17. Which of the following is the correct IUPAC name for the molecule below? CH3 H3C ОН 6-methylheptanoic acid В 6-methylhexanoic acid 6-dimethylhexanoic acid 6-methyloctanoic acid 24 ABCD ABCD
Transcribed Image Text:Page < 5 > of 11 ZOOM + Section A (continued) A14. What is the common name for methylbenzene? Benzonitrile Styrene Toluene Xylene A15. The mechanism of halogenation, nitration, sulfonation, alkylation and acylation of aromatic rings are best described as: Nucleophilic Aliphatic Substitution В A Electrophilic Aromatic Substitution Electrophilic Aromatic Addition Nucleophilic Aromatic Addition A16. Below is a table depicting two examples of nucleophiles capable of partaking in addition reactions with carbonyl groups. Complete Table 1, below, by assigning 1-4. Table 1: Nucleophiles for addition reactions to carbonyl groups. Name Nu-H Reagent H2O ROH Nu- 1 Water alcohol 1 = HO-OH; 2 =H¯; 3 = RO-H; 4 = HO- В A %3D 1 = HO-H; 2 = H¯; 3 = RO-H; 4 = HO 1 = HO-H; 2 = OH-; 3 = RO-R; 4 = HO- 1 %3D НО-Н; 2 - ОН;3 — RO-H; 4 %3D RO- %3D A17. Which of the following is the correct IUPAC name for the molecule below? CH3 H3C ОН 6-methylheptanoic acid В 6-methylhexanoic acid 6-dimethylhexanoic acid 6-methyloctanoic acid 24 ABCD ABCD
Page < 4 > of 11 ZOOM + Section A (continued) A10. Which of the following statements is true for an E1 reaction? The rate of an E1 elimination reaction of an alkyl halide depends on the concentration of: the alkyl halide only В A the base only the product the alkyl halide and base D A11. Identify the main product for the following Sn2 reaction. Br NaSEt main product ? A В SEt Br ŞEt SEt A12. Which reagent should be chosen to carry out the following reaction? A MCPBA KMNO4 CrO3 in H2SO4 D HCI in H2O A13. Which of the following is the strongest base? A В H .N. H ZHN
Transcribed Image Text:Page < 4 > of 11 ZOOM + Section A (continued) A10. Which of the following statements is true for an E1 reaction? The rate of an E1 elimination reaction of an alkyl halide depends on the concentration of: the alkyl halide only В A the base only the product the alkyl halide and base D A11. Identify the main product for the following Sn2 reaction. Br NaSEt main product ? A В SEt Br ŞEt SEt A12. Which reagent should be chosen to carry out the following reaction? A MCPBA KMNO4 CrO3 in H2SO4 D HCI in H2O A13. Which of the following is the strongest base? A В H .N. H ZHN
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