Come up with an organic synthesis for propyl 3-methylpentanoate by using any common reagents of your choosing. The only carbon sources that can be used are 3-methyl-1-pentanol and 1-propanol. Please include a sketch in your explanation. Thanks!
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Come up with an organic synthesis for propyl 3-methylpentanoate by using any common reagents of your...
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...
You have toluene, methanol, ethanol, and propanol as C (Carbon) sources and any solvents or reagents necessary to do your synthesis. You must include solvents and reagents for each step and make sure that all C's (Carbons) in your target molecule come from the available alcohols. The target molecule is 3-benzyl-2,3-pentanediol
Suggest a synthesis of 1, using as starting materials the Her o CO,Et es -CHO 4. a) Lily aldehyde (1) is an ingredient used in perfumery. Suggest a synthesis of 1, using as starting materials, the ester 2 and 1-propanol. You may use any other applicable inorganic and/or organic reagents, but LiAIH, NaOH (aq). PCC, H2, DIBAL, and Pd/C are the most likely choices (depending on your synthetic route). No reaction mechanism(s) is required. Lily aldehyde b) Using 2-methyl-1,3-cyclopentanedione, acetaldehyde...
1) Using 3-methyl-1-butene as the only source of carbon, and any other reagents, outline a synthesis for each compound a) 3 b) c)
Please help by showing how to do the synthesis for both target molecules! Thank you and please be very thorough with explaining the solvents used and please also provide a retrosynthetic anaylsis with the forward anaylsis. Thanks! 7. (16 pts) Synthesize the target molecules using only the carbon sources provided and any reagents of your choosing. Target Molecules Carbon Sources Br Br HO CH3 CH
9) (marks = 3) Provide a reasonable multistep synthesis of the following molecule from the indicated starting material, using any reagents necessary. Please include both a retrosynthesis and a forward synthesis (that includes the product and reagents of each individual step in your synthesis). Meo. = Me Me as a racemic mixture These reagents are your only sources of carbon and both are to be used at different steps of your synthesis
From propane as the only starting carbon source, synthesize 3-propoxyhexane. (please show synthesis of any organic reagents which appear in the final product)
ii. Provide a synthesis of the following the compound below, using 1-propanol and carbon dioxide as your ONLY sources of carbon atoms. More than one step is required. You do NOT need to show the mechanism. You can use any other reagents that you desire. [6 marks]
| -COEU CHO 4 = 4. a) Lily aldehyde (1) is an ingredient used in perfumery. Suggest a synthesis of 1, using as starting materials, the ester 2 and 1-propanol. You may use any other applicable inorganic and/or organic reagents, but LiAlH, NaOH (aq). PCC, H2, DIBAL, and Pd/C are the most likely choices (depending on your synthetic route). No reaction mechanism(s) is required. Lily aldehyde О Мете b) Using 2-methyl-1,3-cyclopentanedione, acetaldehyde and acetone as your only sources of carbon,...
please show all steps and explanation 3 3. (a) Using an acetoacetic ester of your choice and any other needed reagents/reactants, propose the synthesis of:a yheol bebivong elehetem nheta erll onieu A bnuoqmao to 2i2stne MI ( beiupe1 ton e16 2m2insrdoemnoitbs99 ( ) 3,6-Dimethyl-2-heptanone. (i) 2,5-Hexanediol (b) Using a dialkyl malonate of your choice propose an efficient synthesis of: () 2-Benzyl-1,5-pentanedioic acid. (i) 4-Methyl-1-pentanol