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.
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In the box provided draw the structure of the fatty acid formed upon hydrolysis of the fat using dilute acid.
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.
In the box provided, draw the two stereochemical products formed when the ketone shown is reduced with sodium borohydride followed by water. Show correct stereochemistry using wedge-dot structures.I need to see the mechanism for this.3 (4).jpg
Draw the products formed when the reactions are hydrolyzed with dilute acid9-5.jpg
14. Draw an unsaturated fatty acid with that is unsaturated at carbon #2. (You do not need to name it.) 15. Draw glycerol and a fatty acid. Show the mechanism for attachment. 17. Snakes, and particularly poisonous snakes, are awesome. I AGREE I DISAGREE (choose one) What class of enzymes do they use to rock your world when they bite you? What do you think happens to your cells (red blood cells, specifically) as you writhe on the ground in...
I'm not sure how to draw the mechanism such as the electron moving and so on. The structure of triethanolamine is N(CH2CH2OH)3. Steric acid is an 18-carbon saturated fatty acid. Write the mechanism for the acid-base reaction between triethanolamine and stearic acid. Name the salt formed
1. draw the structure of the product of the enamine formed
between cyclohexanone and morpholine
2. draw the structure of the Michael addition product
3. draw the structure of the final product
This question has multiple parts. Work all the parts to get the most points. The Stork reaction is a condensation reaction between an enamine donor and an a,B-unsaturated carbonyl acceptor. The overall reaction consists of a three-step sequence of 1. formation of an enamine from a ketone, 2....
Trimyristin is a fatty acid ester of myristic acid and glycerol. Draw the structure of the products of the base-catalyzed hydrolysis of trimyristin. Using this reaction, calculate a theoretical yield if you started with 1 g of trimyristin. Upload a picture showing all of your calculations. In our experiment we used 50mL of DCM and then refluxed and preformed a distillation to removed the excess DCM. We then used cool acetone to wash the crystals and then did vacuum filtration.
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
In the boxes provided, draw the structures of the two intermediates and the one organic product formed in the following reaction.I need to see the mechanism to get the answers.
Using the Henderson-Hasselbalch equation, determine at what pH the ratio of amine to ammonium ion will be 1 to 100. Write your answer in the box provided.I need to know how to get the answer.3 (17).jpg