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- carry out the mechanism for the acid catalyzed hydrationComplete part 2 of the question (I already did part 1) as explained in the image.4. Write a detailed mechanism for the following reaction. Draw structures of the expected (another method for preparation of alcohols: Review organic I, product. chapter 8) H₂O* Major product Minor product
- what did i do wrong here. , it seems to be marking it wrong but i thought it needed to be protonated2. Show how you could complete the following preparation in two steps. 'Ph OHFour of the seven steps in the mechanism for this process are shown in the conversion of acetal A to hemiacetal E. a.) Add curved arrows for each step b.) Draw another resonance structure for C.c.) Identify the nucleophile and electrophile in Step [3].d.) Which steps are Brønsted–Lowry acid–base reactions?
- Give detailed Solution with explanation needed..identify reagents that complete the reactionPlease don't provide handwrittin solution....Identify the sequence of curved arrows (electron movement) in the steps of the following two separate reactions. a. proton transfer, proton transferb. proton transfer, loss of a leaving groupc. proton transfer, nucleophilic attackd. nucleophilic attack, proton transfer
- Give a clear explanation handwritten answer...complete the following reactionGive the reaction mechanism for ETHYNE and bromine solution. Draw and explain the steps of the reaction mechanism.Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C. ... NH2 HCI/H₂O reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one. + 4 n [ ?
