2 For each of the following, circle the correct choice to indicate (i) if the substituent would activate or deactivate benzene in EAS reactions (ii) is an ortho/para director or a meta director in EAS reactions. a. b. d. di f. g. h. P Substituent Activating or Deactivating (circle one) Activating -CH; है -OH CEN CH3 -Br -N-CH3 CH3 CH₂ -CH₂ CH₂ & CH₂ Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Directing Effect (circle one) Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta

2 For each of the following, circle the correct choice to indicate (i) if the substituent would activate or deactivate benzene in EAS reactions (ii) is an ortho/para director or a meta director in EAS reactions. a. b. d. di f. g. h. P Substituent Activating or Deactivating (circle one) Activating -CH; है -OH CEN CH3 -Br -N-CH3 CH3 CH₂ -CH₂ CH₂ & CH₂ Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Activating Deactivating Directing Effect (circle one) Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta Ortho/para Meta

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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Which reagents can be used to achieve synthesis of the indicated target molecule? Conc. KMNO4/ H* / acetone 1) O3/ Zn/H* 2) PCC/CH2Cl2 O 1) Conc. KMNO4 /H* 2) LIAIH4/THF 4) H3O* 1) Conc. KMNO4, 2) HBr, 3) Mg/ether, 4) CO2 O3/ Zn/H*
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1. When the ketone below is treated with methylmagnesium bromide, two products are formed. Based on your knowledge of addition reactions to ketones, propose a stepwise mechanism that explains the formation of both products. Be sure to include all lone pairs and formal charges. 1. MeMgBr (1 equiv) ....OH ..*** 2. H3O* OH
e. Name the major product/s of this reaction only. 1,2,2-trimethylcyclopentan-1-ol is heated in aqueous sulfuric acid f. (3S, 4S)-4-methyl-3-hexanol is heated in aqueous sulfuric acid
Please solve and explain the answer.
Please don't provide handwriting solution
Show a complete arrow pushing reaction mechanism for the reaction below.
e. Name the major product/s of this reaction only. 1,2,2-trimethylcyclopentan-1-ol is heated in aqueous sulfuric acid f. (3S, 4S)-4-methyl-3-hexanol is heated in aqueous sulfuric acid