Page <5> of 11ZOOM+Section A (continued)A14. What is the common name for methylbenzene?BenzonitrileStyreneTolueneXyleneA15. The mechanism of halogenation, nitration, sulfonation, alkylation and acylation ofaromatic rings are best described as:Nucleophilic Aliphatic SubstitutionВAElectrophilic Aromatic SubstitutionElectrophilic Aromatic AdditionNucleophilic Aromatic AdditionA16. Below is a table depicting two examples of nucleophiles capable of partaking inaddition reactions with carbonyl groups. Complete Table 1, below, by assigning 1-4.Table 1: Nucleophiles for addition reactions to carbonyl groups.NameNu-HReagentH2OROHNu-1Wateralcohol1 = HO-OH; 2 =H¯; 3 = RO-H; 4 = HO-ВA%3D1 = HO-H; 2 = H¯; 3 = RO-H; 4 = HO1 = HO-H; 2 = OH-; 3 = RO-R; 4 = HO-1 %3D НО-Н; 2 - ОН;3 — RO-H; 4 %3D RO-%3DA17. Which of the following is the correct IUPAC name for the molecule below?CH3H3CОН6-methylheptanoic acidВ6-methylhexanoic acid6-dimethylhexanoic acid6-methyloctanoic acid24ABCDABCD Page <4> of 11ZOOM+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 theconcentration of:the alkyl halide onlyВAthe base onlythe productthe alkyl halide and baseDA11. Identify the main product for the following Sn2 reaction.BrNaSEtmain product ?AВSEtBrŞEtSEtA12. Which reagent should be chosen to carry out the following reaction?AMCPBAKMNO4CrO3 in H2SO4DHCI in H2OA13. Which of the following is the strongest base?AВH.N.HZHN

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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

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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