Q: An achiral triglyceride was hydrolyzed to yield one equivalent of palmitic acid
An achiral triglyceride was hydrolyzed to yield one equivalent of palmitic acid and two equivalents of lauric acid. Draw the structure of the triglyceride.
See AnswerQ: Draw a mechanism for the transesterification of tristearin using methanol in the
Draw a mechanism for the transesterification of tristearin using methanol in the presence of catalytic acid.
See AnswerQ: Draw the products obtained when triolein undergoes transesterification using isopropyl alcohol in
Draw the products obtained when triolein undergoes transesterification using isopropyl alcohol in the presence of catalytic sulfuric acid.
See AnswerQ: The conversion of triglycerides into biodiesel can be achieved in the presence
The conversion of triglycerides into biodiesel can be achieved in the presence of either catalytic acid or catalytic base. We have seen a mechanism for transesterification with catalytic acid. In cont...
See AnswerQ: 85. What is the relationship between the following two carbohydrates?
85. What is the relationship between the following two carbohydrates? a. Enantiomers b. Diastereomers c. Resonance forms d. Constitutional isomers 86. Which of the following structures represents...
See AnswerQ: A lecithin was hydrolyzed to yield two equivalents of myristic acid.
A lecithin was hydrolyzed to yield two equivalents of myristic acid. a. Draw the structure of the lecithin. b. This compound is chiral, but only one enantiomer predominates in nature. Draw the enant...
See AnswerQ: A cephalin was hydrolyzed to yield one equivalent of palmitic acid and
A cephalin was hydrolyzed to yield one equivalent of palmitic acid and one equivalent of oleic acid. a. Draw two possible structures of the cephalin. b. If the phosphodiester was located at C2 of th...
See AnswerQ: Draw the resonance structures of a fully deprotonated phosphatidic acid.
Draw the resonance structures of a fully deprotonated phosphatidic acid.
See AnswerQ: Octanol is more efficient than hexanol at crossing a cell membrane and
Octanol is more efficient than hexanol at crossing a cell membrane and entering a cell. Explain.
See AnswerQ: Would you expect glycerol to readily cross a cell membrane?
Would you expect glycerol to readily cross a cell membrane?
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