Problem 6 In the synthesis of lansoprazole, 2,3-dimethylpyridine is converted to the compound shown. Propose a...
the most efficient synthesis possible 6. Synthesis propose to make the compound shown below Starting from benzene. Be sure to include appropriate reaction conditions and products for each step. Steps HO NHL
organic chemisty. questions 2,3 and 4 2. (8pts) Propose a method to convert 2-butyne to the isomers of the compound as shown below. Include any applicable mechanisms and stereochemistry. H OH CH3 Br CH₃ + CH3C=CCH3 Hij H3C он н BrH 3) (8pts) Starting with the compound shown and any other reagents needed, propose a reasonable synthesis for the following compound and include the complete mechanism for your proposed reactions. You must include stereochemistry for full credit. CH3 CH3 H3C-c=c-CH3...
starting with benzene, propose a reasonable synthesis of the following compound. propose a reasonable synthesis of the following compound. NO2
Problem 6 (10 pts) Propose a synthesis of the molecule shown below from cyclohexanol and 1-butanol using any other reactions necessary to prepare intermediates O.
Organic Chemistry Synthesis. Using any necessary reagents. Propose a synthesis for this compound compound.
Propose a simple synthesis for the compound shown below, using the provided starting material and any organic or inorganic Reagent. Draw all intermediates. (Use alkene and alkyne reactions)
Part 2: 1) Starting with a compound with 6 (or less carbons) propose a synthesis for the assigned compounds. Provide all reagents and show intermediates (3 points) COOH CYNO
Propose an efficient synthesis of the compound shown below, starting from acetylene and methyl iodide. You may use any other reagents as necessary, but all carbons in the product must originate from acetylene and methyl iodide.
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.
Starting with benzene propose both a retrosynthesis and a stepwise synthesis for the following compound. Starting with benzene propose both a retrosynthesis and a stepwise synthesis for the following compound.