5. Propose a synthesis of each of the following compounds using the indicated starting material. You may use any organic compounds, inorganic compounds, organometallic compounds, or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. a. H3C steps OH F3C CI (racemic) F3C Ph

5. Propose a synthesis of each of the following compounds using the indicated starting material. You may use any organic compounds, inorganic compounds, organometallic compounds, or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. a. H3C steps OH F3C CI (racemic) F3C Ph

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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4. Propose a synthesis of each of the following compounds using the indicated starting material. You may use any organic compounds and any inorganic compounds or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. a. b. C. CH3 Ph steps Ph CI steps ACHO -CH3 CN steps Ph Ph -OH (racemic)
5. Propose a synthesis of each of the following compounds using the indicated starting material. You may use any organic compounds, inorganic compounds, organometallic compounds, or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. a. H3C steps OH (racemic) F3C CI FaC Ph b. H3C CH3 C. steps H3C CH3 B -H CH3 NH₂ steps (racemic)
4. Propose a synthesis of each of the following compounds using the indicated starting material. You may use any organic compounds and any inorganic compounds or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. a. b. C. H3 -CH3 steps Ph Ph steps 4 CN steps -CH₂ Ph Ph -OH (racemic)
5. Propose a synthesis of each of the following compounds using the indicated starting material. You may use any organic compounds, inorganic compounds, organometallic compounds, or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. a. b. C. Ph + PPh3 Cl mylom Ph. CH3 steps steps steps H3C. H3C Ph CH3 CH3 Ph OH ÕH Ph (racemic) 4
9. Propose a synthesis of each of the following compounds using the indicated starting material. You may use any organic compounds and any inorganic compounds or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. Ina b. steps CH₂ CH₂ en Ga CH₂ OCH₂ steps (racemic)
In synthesis shown in box, which of the following reagents is expected to give the indicated product ? 1. in high yield? HO. 2. HС, Н,О A) LIAIH4 B) NaH C) NABH4 D) SOCI2 A OD B.
Propose a synthesis of each of the following compounds using the indicated starting material. You may use any organic compounds and any inorganic compounds or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. a. b. J H3C steps CH3 H3COH Ph CH3 steps steps -CEN H3C H3COH Ph CH3 OH OH (racemic)
Draw the major organic product of the following reactions. Include all arrows and steps BV NA OCH3 CH3OH 1. LDA 2.
Provide the major organic product of the reactions shown below. ShowN the produ from each step shown below. 1. NayCryO7 2. SOCIE 3. CH,OH, H", A
Arrange the compounds below in order of increasing reactivity in a SN2 reaction. 1. (CH3)2СНCI 2. CH3CH2B1 3. CH3CH2C1 A) 1; 2; 3 В) 3;B 2; 1 C) 1; 3; 2 D) 2; 1; 3 E) 3; 1; 2
7. Identify compounds B-G according to the following synthetic scheme. A CH₂Br Mg ether B D D₂O 1. acetone 2. H₂0 C conc. H₂SO4 heat E ex H₂ Pt 2 eq. Br2₂ G F
10. Alkyl diazonium salts decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes) rearrangement. Keeping this in mind, draw a stepwise mechanism that forms all of the following products. NaNO2 HO + `NH2 HCI, H2O HO,