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1 and 2 1) Starting from 1-methylcyclohexane-1-ol, devise a synthesis for (18,2R)-2-methylcyclohexan-1-ol. (3 points) "OH "он...
5. Devise a synthesis of each product from the given starting material. More than one step is required. он он OCH а. OH C. Br Br d. (CHa)2CHCH CH-C-CH,Br b. CH-C-CH (CH3,сCI н
6. (18 points total) Synthesis: Devise a synthesis of the following compound from the given starting materials. You may use any other organic or inorganic reagents you deem necessary but you must use the given starting materials as your only source of carbon in the final compound OH several steps OH MeOH HO
3. Devise a multi-step synthesis of the target molecule from the given starting material. Show all necessary reagents and conditions for each step and the product of each step. (7) OH
Devise a synthesis of (Z)-3-octene 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 нсисынсно-си нос-сцен нос-cң соң,он нонс Reagents + NaNH / NH diodo ethane 1-bromo-3-methybutane H undar catalyst + NaOH HẠO e 1-bromopropane butyl bromide күн clodomethane 1 2-bromopropane H/Pd on carbon I N/NH0 Starting material Reagent for step 1...
12. (4 points) Devise a synthesis and show the mechanism (unless it is hydrogenation or hydroboration) for each product from the given starting material. More than one step is required for each both products will form
12. (4 points) Devise a synthesis and show the mechanism (unless it is hydrogenation or hydroboration) for each product from the given starting material. More than one step is required for each both products will form
Question 2 us Devise a synthesis of each product from the given starting material. More than one step is required a. OH OH Br b. OCH d. e. In the box below, write down what time displayed your answer to the webcam. Be sure to leave it up for 3-8 seconds. Please make sure you follow the formatting guide given to you near the topat this page BI VAA. IE3XXE - Page
Devise a synthesis of the following compound from styrene (CH3CH=CH). You may use any inorganic or organic reagents. More than one step is required. CH3CH2COOH Part 1 out of 2 CHECH=CH2 12] H202, OH
3. Devise a multi-step synthesis of the target molecule from the given starting material. Show all necessary reagents and conditions for each step and the product of each step. (7) OH BONUS: Please provide the arrow pushing mechanism of this reaction. Be sure to show a charges and stereochemistry where needed. To receive full credit, what is the name of this reaction? (4) NaOE HOE Br
Chem2020 Provide a multistep synthesis to accomplish the following transformations. Be sure to show all starting materials, reagents, reaction conditions, and products for each step. Each synthesis will be more than 1 step. +2 CO HO. OH c Chem2020 Provide a multistep synthesis to accomplish the following transformations. Be sure to show all starting materials, reagents, reaction conditions, and products for each step. Each synthesis will be more than 1 step. +2 CO HO. OH c