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Please Write out the mechanism for the multistep synthesis below
![2. Perform the maltep synthesis below?
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- Please try to give type solution fast in 5 mins i will rate for sureCircle the correct answer in each sentence. Projection 1 is a (boat ; fischer ; haworth ; sawhorse) projection. Projection 2 is a (boat ; fischer ; haworth ; sawhorse) projection. This sugar is a (pentose ; hexose) and is a (aldose ; ketose). It is classified as a (simple ; complex) carbohydrate. This is the (L- ; D-) enantiomer of this sugar.Show the synthesis for this reaction
- 1.Activity electron substituent increase with withdrawing?what does it means?does it means when NO2 ,CI ,Br is attached on that ring will increase the activity or without NO2 ,CI ,Br is attached will be better?? Please type!No hand writing!help with my ochem homeplease3. Atazanavir (structure below) is an orally delivered AIDS-drug which works as an inhibitor for the HIV aspartyl protease. OH Meo. .N. N. OMe `Ph Atazanavir i) Draw the high energy intermediate of an aspartyl protease-catalysed cleavage of the amide bond in the peptide R1-CO-NH-R?. ii) How well does Atazanavir follow the Lipinski's rules of five (log P 4.5)? IZ IZ
- Q 36,37,38 Can someone help me with these please? Please ignore selected answer even if right and label answers clearly. Thanks so much!! :)Hi I don't really understand the answer to this question... Is it possible you would explain it more thoroughly? Problem: Examination of the cleavage of the amide substrate, A, by chymotopsin with the use of stopped-flow kinetic methods reveals no burst. The reaction is monitored by noting the colur produced by the release of the amino part og the substrate (highlighted in orange). Why is no burst observed?Utilize the carbohydrate provided to answer each part below. a. On the Fischer projection, clearly circle the penultimate carbon. b. Circle the appropriate name listed below that corresponds to the structure.• D-aldopentose • D-aldohexose • D-ketopentose • D-ketohexose • L-aldopentose • L-aldohexose • L-ketopentose • L-ketohexose
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