a. Identify the reagents that can be used to covert benzene into each of the following compounds? Conversions need more than one step. Draw the reactions i. m-chloro ethyl benzene ii. Methyl benzoate
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Identify the reagents that can be used to covert benzene into each of the following compounds? Conversions need more than one step.
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- What is the major organic product of the following reaction? (Assuming excess reagents) O A OB O C A. OD B. Problem viewing the image. Click Preview Here C. C. D. O O O :0 Zn(Hg) HCI/H₂O OH19. Mechanism cat. TSOH H. CH;OH1. Draw the products of each nucleophilic substitution reaction a. b. D b OH C. d. e. f. Br 1 NaCN + NaOCH3 H₂O
- In Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 See Periodic Table O See Hint :ö: :Br: Add the missing curved arrow notation. 20 F CI Br I Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Keg > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e. Keg « 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg« 1) because bromide is a better leaving group than acetate.027 In Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 4 See Periodic Table O See Hint :0: :Br: Add the missing curved arrow notation. S CI Br Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Kea > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e., Keq« 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg 1) because bromide is a better leaving group than acetate. +1.does acetylsalicylic acid can hydrogen bond witha. itselfb.water2. determine the electrophilic and nucleophilic of acetylsalicylic acid
- For esch of the following two reactions draw the major product. Br,, hv KMNO, heatO#1 Draw all possible constitutional isomers formed by DEHYDROHALOGENATION of each alkyl halide. Br CI Br b. а. С. d.48. Which set of reagents would accomplish this conversion H. H. CH3OH with H* as a catalyst NaH followed by CH3OH CH3ONA followed CH3OH CH3ONA followed by CH3Br a. b. C. d.
- Synthethic pathway with intermediates and reagents plz.Synthesize each compound from cyclohexanol using any other organic or inorganic compounds. CH,OH a. g. (Each cyclohexane ring must come from cyclohexanol.) COOH b. d. h. сно CHs (Each cyclohexane ring must come from cyclohexanol.)Alkenes and alkynes behave like and thus attract. nucleophiles ; electrophiles B nucleophiles; nucleophiles C electrophiles; nucleophiles D electrophiles; electrophiles