Draw the structure of the product formed when the sugar below is oxidized using nitric acid to produce an aldaric acid. On the line provided, indicate whether the product is optically active (O.A.) or optically inactive (O.I.).
Show the mechanism
Draw the structure of the product formed when the sugar below is oxidized using nitric acid to produce an aldaric acid. On the line provided, indicate whether the product is optically active (O.A.) or optically inactive (O.I.).
Draw the structure of the products formed when the sugar below is reacted with sodium borohydride followed by water. On the lines provided, indicate whether each product is optically active (O.A.) or optically inactive (O.I.).Show the mechanism.
Compound A is a D-aldopentose that can be oxidized to an optically active aldaric acid B. On Kiliani-Fischer chain extension, A is converted into C and D; C can be oxidized to an optically inactive aldaric acid E, but D is oxidized to an optically active aldaric acid F. What is the structure of compound C? PLEASE SPECIFY WHAT IS COMPOUND C Also please take into account the instructions for the answer shown Compound A is a D-aldopentose that can...
2. Draw the major product(s) formed when the optically active compound shown below is treated with H2O/H2SO4. Is the product optically active? Why or why not? (4 pts) optically active
draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOH3. Indicate the stereochemistry of the product. explanations are highly appreciated. thank you. (please show answer with dash and wedge) Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NAOCH3. Indicate the stereochemistry of the product Interactive 3D display mode CH3 CH3 Н.С" Br ШИ
2. Draw the structure of the major organic product that is formed from the following reaction. Draw this structure in the box at the bottom of the next page. Then use letters to label all the sets of chemically equivalent carbons in this structure. The broadband proton-decoupled 13C NMR spectrum of the product is shown below. DEPT 90 and DEPT 135 data are included in the table on the following page. Use this spectroscopic data to make clear assignments of...
In the box provided draw the structure of the fatty acid formed upon hydrolysis of the fat using dilute acid.I need to see the mechanism to get answer.3 (14).jpg
Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOCH3. Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOCH3. Indicate the stereochemistry of the product.
In the box provided draw the structure of the salt formed when the acid shown is reacted with sodium bicarbonate.I need to see the mechanism to get the answer.
Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOCH3. Indicate the stereochemistry of the product. Interactive 3D display mode CH CH CI Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. CI Br Submit Previous Answers Previous Answers Request Answer x Incorrect; Try Again; 4 attempts remaining rovide Feedback Next
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...