5. Starting with a compound having no more than 6 carbons make the given molecules following...
5. Starting with a compound having no more than 6 carbons make the given molecules following the specific instructions for each one. While mechanisms are not needed here, please make sure you write out the reagents and products of every step. (5 5) a. Use a Grignard reaction in one of the steps OH b. Use the Gilmann reagent in one of the steps
Please solve all the problem questions Propose a synthesis for compound with certain the following reagents. Grignard reagent Geranial, citral (3,7-dimethylocta- 2,6-dienal ) OH Product / Identify the complete reaction with all reagents and products in addition to the reaction mechanisms ✓ Reference the bibliography used, (scientific Jounal articles) ✓ Describe step by step the synthesis methodology in laboratory.
51. Make the following compound from the starting reagent. Show all the steps, reagents involved and the intermediate products. a. 7 بل mynd OH b. Synthesize the following molecule from benzene via a diazonium salt. Show all the reagents and the intermediate products. COOH OH c. Synthesize the following amine from the given alkyl halide in good yield. Show all the intermediates and reagents. CHE
9.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You may use any other organic reagents or inorganic reagents you wish. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate), and products of each synthetic step but NO MECHANISMS. [4 points) OH Use to make HO
9. P ropose a multi-step synthesis to accomplish the overall transformation shown below (make the molecule on the right starting with the molecule on the left). Show all necessary reagents and products for each forward step. [It is not necessary to show any mechanisms.] OH 10. Propose a multi-step synthesis to accomplish the overall transformation shown below (make the molecule on the right starting with the molecule on the left). Show all necessary reagents and products for each forward step....
QUESTION 12 Prepare the compound shown below from cyclohexanone (use as many molecules as needed) and organic compounds of three carbons or less as the starting materials. Show the product of each synthetic step and indicate all necessary reagents and reaction conditions. Count carbons carefully! os
Please explain the mechanisms! 1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Multiple steps are required. The number of steps you use does not matter. Reactions should give the desired product as a major product. For full credit show the product of each step (reaction). If you make use of organometallic reagents such as Grignard, Wittig, organolithium, organosodium, organocopper, etc. you must...
Please answer all parts for good rating! The following reaction will not result in complete conversion to the amide compound. Suggest all of the products (the main organic products as well as any by-products) and indicate the number of moles of each product formed and the approximate number of moles of each reagent remaining. The reaction takes place in an inert (non-reactive) solvent. NH u. CI 1.0 mol 1.0 mol Suggest the reagents and steps needed to synthesize the following...
i get to the product but always add 6 carbons! how do i make it with 5 carbons? Synthesize starting from Benzene. Can add reagents up to 5 carbons long. Use at least one Organometallic reaction to create. Synthesize starting from ethene. Can add reagents up to 5 carbons long.
Propose the most efficient synthetic route to make the following compound starting from the indicated reagents and any other reagents, clearly identifying the reaction conditions at each step and the structure of the intermediates formed. Propose the most efficient synthetic route to make the following compound starting from the indicated reagents and any other reagents, clearly identifying the reaction conditions at each step and the structure of the intermediates formed. *Note: This will require more than 3 steps* ohin 3...