5. Using bromobenzene, cyclohexene and vinyl bromide as your source of carbons, outline a synthesis of...
5. Using bromobenzene, cyclohexene and vinyl bromide as your source of carbons, outline a synthesis of 1-cyclohexyl-2-phenylethanol which is used to reduce irritation in transdermal drug delivery (15 pt) By o 7or -
N H OH H2O OHO Ising hromobenzene, cyclohexene and vinyl bromide as your source of carbons, outline a
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...
Question 6. (14 marks) Using reactions taught in class, outline a synthesis to produce 3,8-dimethyldecan- 4,7-diol shown below. You may only use 2-bromobutane as a carbon source for your synthesis, but you may use any inorganic reagents you wish for the synthesis, which will require several steps. For full marks, provide the reagents to each step, and provide each compound synthesized in the production of the final target molecule. You may ignore stereochemistry for this question. If you need extra...
Integrated Problem 09.64 Using acetylene and methyl bromide as your only sources of carbon atoms, propose a synthesis for the following compound: + En A Choose from the following list of reagents (A-H): 1) Br2 2) Excess H20 3) NaNH2 1) H2, Lindlar's catalyst 2) HBr 1) NaNH2 2) EtBr 3) Na, NH3 (1) 4) MeBr 1) NaNH2 2) EtBr 3) NaNH2 4) MeBr H 1) Na, NH3 (1) 2) MCPBA 1) NaNH2 2) EtBr 3) H2, Pt 1) H2,...
Question 5: Outline a synthesis for any Two of the following four synthetic transformations. In your answer you should provide all reagents required to effect each transformation and the structures of any neutral intermediate compounds [only the first two answers will be graded] 16 pts, 8 pts each OH 1. a 2. COOH COOH 3. B! HOOC
stepwise synthesis for N-propylbutanamide using 1-propanol and/or carbon dioxide as your only source of carbon Use Using the reagents below, list in order (by letter, no period) those necessary to provide this synthesis. Note: Not all spaces provided may be needed. Hints: First receive a Grignard reagent in steps 1 and 2. Use propanol in step 5. In step 9 a product from step 4 reacts with a product from step 8. a. NH3 b. Mg/ether c. SOCl2 d. 1....
X Incorrect. The synthesis above used bromobutane, but acetylene is the only allowed source of carbon atoms. Using the reagents given, identify a synthetic route for the production of bromobutane from acetylene. ? H Br The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagent(s) in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide...
please help with how the flow chart will look like? thank you! Synthesis of n-Butyl Bromide Purpose of the Experiment: In this week's experiment you will be synthesizing n-butylbromide (IUPAC 1-bromobutane from 1-butanol and a concentrated acid via a nucleophilie substitution reaction. It is important to know that alcohols dehydrate to form alkenes in the presence of strong inorganic acids, so care must be taken in this experiment not to heat the reaction too vigorously else an elimination reaction may...
Question 3 Propose a stepwise synthesis for N-propylbutanamide, using 1-propanol and/or carbon dioxide as your only source of carbon and any other reagents necessary. Testbank, Question 140a Using the reagents below, list in order (by letter, no period) those necessary to provide this synthesis Note: Not all spaces provided may be needed. Hints: First receive a Grignard reagent in steps 1 and 2. Use propanol in step 5. In step 9 a product from step 4 reacts with a product...