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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 =
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
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