4. Propose a synthesis of the compound on the left from the indicated starting material and...
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
Propose a synthesis of the target compound from the indicated starting material. (Answer any two problems for full credit)
Devise a synthesis of the following compound from the indicated starting material, organic compounds containing one or two carbons, and any other required reagents. Be sure to answer all parts. Devise a synthesis of the following compound from the indicated starting material, organic compounds containing one or two carbons, and any other required reagents. Be sure to answer all parts. (+ enantiomer) CECH edit structure ... CH,CI edil structure. edit structure
4) Propose a synthesis for cach product from the provided starting material and any other reagents needed. Br N,N-diethyl-m-toluamide (DEET) OH
5. Provide a synthesis for each molecule shown below starting from the indicated compound. In addition to the starting material, you may use any necessary reagents. OH a. Eto Et
propose a synthesis mechanism and reagents that will yield this product from the indicated starting material ܐܘ COH
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
6. (18 points total) Synthesis: Devise a synthesis of the following compound from the given starting materials. You may use any other organic or inorganic reagents you deem necessary but you must use the given starting materials as your only source of carbon in the final compound OH several steps OH MeOH HO
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.
Propose a synthesis of the following molecule starting with the indicated starting molecules as the only allowed carbon sources and any needed inorganic reagents. Br B(OH)2 + ethyne ethyl iodide