Give the major product(s) of the following reactions, if there is a reaction. For electrophilic aromatic substitution, assume that only one equivalent of the electrophile adds to the aromatic ring (monosubstitution). However, there may be more than one product formed. HNO3 H2SO4 OCH3 F H2SO4 NH2 1) H3C AICI3 2) H20 CI Cl2 FeCl3 `NH3

Give the major product(s) of the following reactions, if there is a reaction. For electrophilic aromatic substitution, assume that only one equivalent of the electrophile adds to the aromatic ring (monosubstitution). However, there may be more than one product formed. HNO3 H2SO4 OCH3 F H2SO4 NH2 1) H3C AICI3 2) H20 CI Cl2 FeCl3 `NH3

Chemistry

10th Edition

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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BS21008 Organic Chemistry for the Life Sciences Assignment Week 7 Bearing in mind Huckel's rule, determine whether each of the heterocycles involved in the following acid-base equilibria is aromatic or not (show your working). Use your findings to explain which of the nitrogen atoms in the indazole ring is more basic, i.e. which would be the product of indazole protonation, compound A or compound B? + H* + H* N: - H* - H* H CH3 CH3 CH3 A 1-methyl-1H-indazole
When ethoxybenzene is treated with a mixture of nitric acid and sulfuric acid, two products are obtained, each of which has the molecular formula C8H9NO3. For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do not use abbreviations such as Me or Ph.
What type of substituent effect do you expect a -CC12-CC12-CC13 (perchloropropyl) group to have upon aromatic electrophilic substitution reactions? Resonance electron donor; activating substituent; ortho/para director Inductive electron donating; activating substituent; ortho/para director Resonance electron withdrawing; deactivating substituent; ortho/para director Inductive electron withdrawing; deactivating substituent; meta director
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electrophilic aromatic substitution reactions. type op or m, to indicate if the group would be an op or meta director in b H H H H h H CH3 blank 1 blank 2 blank 3 blank 4 blank 5 blank 6 :O: HLYXHOX CH3 CH₂CH3 blank 7 -CH3 C=N: blank 8 blank 9 blank 10 blank 11
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[Review Topics] [References] Devise a synthesis of butane using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps. Starting materials HCECH HOEC-CH, 1 Reagents 2 a Nanhbinh(D) b NaOH/H₂O c iodomethane Starting material Reagent for step 1 Reagent for step 2 Reagent for step 3 Submit Answer HCEC-CH₂CH₂ 3 diodoethane e 1-bromopropane. f 2-bromopropane Retry Entire Group HCEC-CH₂CH₂CH₂CH₂ 4 g 1-bromo-3-methylbutane h t-butyl bromide i H₂/Pd on carbon CH₂ HCEC-C-CH₂ H 5 9 more group attempts remaining KHINH (1) CH₂ HC=C-C-CH₂ CH₂ jH₂ Lindlar catalyst I Na/NH₂ (D 6 Previous Email Instructor Next Save and Exit
Draw the structure of the starting material needed to make 2-methylhept-3-yne using sodium amide in liquid ammonia, followed by 1-bromopropane. The starting hydrocarbon must have no more than five carbons 1) NaNH2, NH3() NaBr + 2) CHзCH2CH2Br
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a) b) C) Show the steps necessary, in order, to make each of the following compounds. Start with benzene, and use only reactions we studied this semester. O 10₂ NO₂ -ECH₂CH3 o Br
Q2Show why the OH functional group, of phenol below, is ortho directing using curly arrows to show the formation of each of the four resonance structures A, B, C and D. Draw all the resonance structures A through D and explain why one resonance structure is more favourable than the other three in directing the electrophile (E*) ortho to the OH functional group.