What is the major organic product obtained from the following reaction? 1 2 4 3 OH OH 2 Δ OH OH fron 3
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- For the following monosaccharide, draw the products formed when treated with each reagent. H H -OH HO H HO H H― -OH CH₂OH Part 1 of 2 H2 in the presence of a Pd catalyst. Modify the Fischer projection of the monosaccharide to represent the product. H H -ОН HO H HO H H -OH CH₂OH Part 2 of 2 Benedict's reagent. Modify the Fischer projection of the monosaccharide to represent the product. H H -OH HO -Н HO H H -OH CH₂OH ☐ : G ☐ E ☐: ☑ P GFor the following monosaccharide, draw the products formed when treated with each reagent. H. HO H H OH HO H H OH Part 1 of 2 CH₂OH H₂ in the presence of a Pd catalyst. Modify the Fischer projection of the monosaccharide to represent the product. H HO -H H -OH HO -H H -OH CH₂OH Part 2 of 2 Benedict's reagent. Modify the Fischer projection of the monosaccharide to represent the product. HO H H -OH HO H H -OH CH₂OH Q:Please draw the major product(s) of the following reaction and show the mechanism. Is there a reason why one stereochemistry is preferred over the other for this reaction?
- Modify the Fischer projection of the following aldose to show the compound that is formed when the aldose is treated with H2 in the presence of a Pd catalyst. CHO H -OH HO H H .OH CH₂OH X :ロ GComplete the following reaction by filling in the necessary reagents. NH₂ S. 1) Br 2) Draw the product for the following reaction. Η N|H CH 3 1. CH3I (excess) 2. Ag₂O 3. A F BrIn solution, glucose exists predominantly in the cyclic hemiacetal form, which does not contain an aldehyde group. How is it possible for mild oxidizing agents to oxidize glucose?
- What are the products when the following molecule is hydrolyzed using NaOH (soaponification)?Select the aldol condensation product of the following reaction. a A b B с C d D e E A H HO H NaOH, EtOH heat H H B D EDehalogenase enzymes catalyze the clevage of C-X bonds. One such dehalogenase catalyzes the following reaction. An active site aspartate is thought to carry out the initial nucleophilic attack that expels the chloride. Select the most likely intermediate in the reaction. (Note the stereochemistry. Refer to P11.19 in the textbook if needed.) O O A C D OE -CH₂ H H₂C™ CO₂ H B CO₂ CI N H₂O Cr CO₂ H CO₂ нотум CH3 D CO₂ five N E CH₂
- Given the following choices,a. what is the structure of the product of the reaction catalysed by ACAT?b. structure of the product produced from the reaction catalysed by phospolipase A2?c. general structure of TAGd. structure of glycerolDraw the major product of the following Heck reaction. MeO Pd(OAc)2 (1 equiv) AcOH 63% Draw the major product of the following catalytic allylic alkylation Pd(PPh3)4 OAC NaCH (CO2CH3)2(i) During the Pyruvate Decarboxylase (PDC) catalysed reaction, a covalent coenzyme intermediate is formed. On the skeleton of the covalent coenzyme intermediate below draw the appropriate double bonds, charges, and electron pairs to illustrate the two resonance forms of this intermediate. Name each form in the boxes provided. HO S R' N -R HO S R' N -R