4. Propose a synthesis of the molecule below starting with benzene. You should consider using an...
4. Propose a synthesis of the molecule below starting with benzene. You should consider using an arenediazonium salt. (2 points) CH2CH3
1. Propose a synthesis of the molecule below starting with benzene. You can use any other reagents you want. (2 points) сн.CH, но-с-сн, сH;
4. Propose an efficient synthesis of the molecule below starting with benzene. You can use any other reagents you want. NOTE: Some reactions produce ortho- and para-products. It is allowable to just take ONE of the products and use it in the next synthesis or claim it as the final product (we assume that ortho- and para-products can be separated). (3 points) CH2CH2CH Br
Starting with benzene propose a synthesis for the target molecule below. Name the Target Molecule. Target Molecule
Propose an efficient and elegant synthesis of the molecule using only a benzene as your starting material. You may use any alkyl halide or alcohol as your other sources of carbon (excluding HCOCl), and any other reagent you deem necessary. OH Cl
. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) Retrosynthesis HO O 04
3. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) но
3. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) i =
9. Propose an efficient synthesis of each molecule below starting from benzene and any other reagents needed (organic or inorganic) A. CI B. CI NO2 Br
3. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) HO