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- Which of the following molecules is most nucleophilic? OA. NaOCH₂CH3 OB. CH3CH₂OH OC. NaOC6H5 OD. C₂H5OH 1 E.CH3COONaPlease, I need help with the question below. I will rate it Explain which mechanism is predominant in each of the above elimination reactionsand how it affects the product formation. Thank you for your help.b).. .. Under each potential product of this E2 elimination, write "major product," "minor product," or "not formed." Me Br H Me Me OH Me Ph Ph H Me H Et Me Me Me Ph Ph Me Me Et
- Multi-step synthesis. Give the reagents over the arrows and the intermediates between thearrows that are required to synthesize the product compound on the left from the reactant givenon the right for each retrosynthetic analysis.Consider the following reaction. What is the role of LDA? CH2CH3 CHCO Et 1. LDA, THF 2. CH3CH₂Br CHCO₂Et LDA acts as a nucleophile and is substituted by the THF. LDA acts as a base and removes a proton from the alpha carbon to form the enolate. LDA acts as an electrophile and adds to the alkyl halide so it is easier to substitute. LDA acts as an acid to protonate the carbonyl carbon to form a good electrophile.Draw the structure of the final product when p-nitroanisole is sequentially subjected to the following reactions.
- Please help me draw the productsDraw the nucleophile needed to convert 1-bromobutane to the following substance.For SN1 Explain the order in which 1o (primary) alkyl halides reacted (fastest to slowest) and explain why. The 1o primary alkyl halides are: (see picture below) 1-chlorobutane 1-bromobutane 1-chloro-2butene benzylchloride
- 6. Show how to synthesize the target molecule from the given material as the only source of carbon. Show the reagents needed for each step and the product of each step. OH .OHPropose a synthetic pathway for the conversion of each of the indicated starting materials into the respective products EtzN. HO. HO. `CO2E1Complete the diagram of reactions without mechanisms by giving the reaction conditions or the missing product