Please help organic chemistry provide a reasonable reaction mechanism for the following reaction Answer both parts...
ts of the following question. Provide a synthesis of the following substance from the indicated starting materials. You may assume that you have any needed inorganic reagents. diiodomethane methyl iodide allyl bromide benzaldehyde 1-phenylethene Ph ioniem for each step of the following process: ts of the following question. Provide a synthesis of the following substance from the indicated starting materials. You may assume that you have any needed inorganic reagents. diiodomethane methyl iodide allyl bromide benzaldehyde 1-phenylethene Ph ioniem for...
please explain why the answer is the answer step by step Retrosynthetic Analysis Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. If equal mixtures are anticipated (ie. ortho/para products) then indicate...
Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. If equal mixtures are anticipated (i.e. ortho / para products) then indicate where separations are needed. NO MECHANISMS! [6 points 2. Give a...
Provide a stepwise synthesis for the following reaction. you may use the indicated starting materials as well as any organic or inorganic reagents.
Retrosynthetic Analysis 12. Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. NO MECHANISMS! [8 points] NH ONH2 Make starting with
7. MECHANISM: Give the complete stepwise mechanism to account for the following observation. Use curved arrows to show FLOW OF ELECTRONS. [9 points H-CI 8.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. [6 points] OH...
Provide a reasonable yet detailed mechanism for BOTH of the following transformations. Show all key resonance structures for the intermediates generated. at worden dan on no [2 x 7 marks] Propose a practical synthesis for the compounds shown from benzene. Use any other necessary organic or inorganic reagents. Show all intermediates formed to receive full credit. Assume any isomers formed can easily be separated. COOH [9 marks]
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
can someone show me mechanisms please *2 6 points) Provide a reasonable synthesis of each of the molecules shown ang from the indicated starting material, and using any organic or inorganic reagents. The synthesis The synthesis may require more than one sten. You must write the reagents in correct sequence. Remember to work backward from the product starting material. No mechanism. Br ???? LOH OH racemic 1) NO DE+E+0H 2) KMnO4 NaOH cold (or 0504) ???? racemic E- Alkene 1)...
Synthesis 10. Give a reasonable synthesis for the following compound from the indicated starting material. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. NO MECHANISMS! [6 points) Make med og som en ons starting with SO3H