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- SHOW/IDENTIFY the arrow pushing mechanism in at least 4 steps. CH,OPO?- | 3* C=0 2 HO-CH2 1 CH,OPO | 1 C=0 2 Dihydroxyacetone phosphate (DHAP) Но—С H 3 aldolase + Н—С-—ОН H Н-С-—ОН 15 CH-ОРО 6. Н—С—ОН CH,OPO Fructose- 1,6-bisphosphate (FBP) Glyceraldehyde- 3-phosphate (GAP)Propose a mechanism. Br2, H20 H2C=CHCH2CH2CH2OH -CH2B.Please show mw the mechanism for the product
- Rank the compounds in order of reactivity toward nitration with HNO3: benzene 2-methylfuran thiophene Most reactive Least reactive Answer Bank 3-methylthiophenePropose a reaction mechanismThe reaction below is a base-catalyzed aldol reaction. O || CH₂-C-H CH3-C-H Ethanal (Acetaldehyde) H I CH3-C-H Ethanal (Acetaldehyde) NaOH Draw curved arrows to show the movement of electrons in the step of the mechanism shown below. Arrow-pushing Instructions AC⇒x= :O: || :CH₂-C-H OH Bl CH3-CH—CH2-CH -CH₂-1-1 a 3-Hydroxybutanal (B-hydroxyaldehyde; formed as a racemic mixture) :0: :0: || CH3—CH—CH2-C-H A tetrahedral carbonyl addition intermediate X
- CH3NH2 H30* e) j) NaOEt Aldol CondensationDraw the expected major elimination product and identify the mechanism. H3C Br CH3OH Select Draw Templates More / || ||| C → "H O Erase Q2 QMacmillan Learning Predict the major product for the reaction. H Cl₂, CH3CH₂OH Draw the major product. Select Draw Templates More ||||||||||| CH CI O
- When D-glucose is treated with aqueous sodium hydroxide, a complex mixture of carbohydrates is formed, including D-mannose and D-fructose. Over time, almost all aldohexoses will be present in the mixture. Even L-glucose can be detected, albeit in very small concentrations. Using the fewest number of mechanistic steps possible, draw a reasonable mechanism showing the formation of: L-glucose from D- glucose.Draw the expected major elimination product and identify the mechanism. H3C CH3 CH3OH Select Draw Templates More // W C H OO Macmillan Learning Draw the structure of the major organic product of the reaction shown. KMnO4 heat H+ Select Draw Templates More / |||||| J C HO HO