What will be the complete hydrolysis products of the given structure below? CH2 -o-c C17H37 HC-O-C-C,7H29 0--0-CH;CH2N° C H3)3 O yield 1 mole of fatty acid, sphingosine, phosphoric acid & choline upon hydrolysis O yield 1 mole of fatty acid, glycerol, phosphoric acid & choline upon hydrolysis O yield 2 moles of fatty acid and 1 mole of sphingosine, phosphoric acid & choline upon hydrolysis O yield 2 moles of fatty acid and 1 mole of glycerol, phosphoric acid & choline upon hydrolysis

What will be the complete hydrolysis products of the given structure below? CH2 -o-c C17H37 HC-O-C-C,7H29 0--0-CH;CH2N° C H3)3 O yield 1 mole of fatty acid, sphingosine, phosphoric acid & choline upon hydrolysis O yield 1 mole of fatty acid, glycerol, phosphoric acid & choline upon hydrolysis O yield 2 moles of fatty acid and 1 mole of sphingosine, phosphoric acid & choline upon hydrolysis O yield 2 moles of fatty acid and 1 mole of glycerol, phosphoric acid & choline upon hydrolysis

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter27: Biomolecules: Lipids

Section27.SE: Something Extra

Problem 41AP

See similar textbooks

Similar questions

Identify the organic functional group of the reactant and the reaction type then predict the functional group(s) of the product(s).The reactant is a(n)a. ketoneb. esterc. amided. alcohole. carboxylic acidf. amineg. aldehydeThe reaction type isa. hydrationb. hydrolysis (in base)c. esterificationd. dehydratione. hydrolysis (in acid)f. amide synthesisThe product should be a(n)a. ketoneb. aldehydec. alcohol onlyd. estere. carboxylic acid and an alcoholf. carboxylic acid onlyg. amide
What is the product of the starting material D-glyceraldehyde which will (1) produce aldaric acid upon reacting with HNO3 + H2O, NaOCH2, NH2OH, and (CH3CO)2O + NaOCOCH3 (2) produce tartaric acid upon reacting with HNO3 + H2O, NaOCH3, NH2OH, and (CH3CO)2O + NaOCOCH3
What is the name of reaction 1? How about the name of reaction 2? a Hydrolysis b Aminolysis c Alcoholysis d Reduction Which of the following is product B? a methyl 2-bromobutanoate b 2-bromobutanoic acid c 2-bromobutanamide d 3-bromobutan-1-ol
Identify the organic functional groups and reaction type for the following reaction.The reactant is a(n) a. amideb. aldehydec. alcohold. carboxylic acide. esterf. ketoneThe product is a(n)a. carboxylate ionb. ammonium ionc. alcohold. carboxylic acide. ketonef. aldehydeThe reaction type isa. hydrationb. esterificationc. hydrolysis (in acid)d. hydrolysis (in base)e. amide synthesisf. amide synthesisg. dehydrationh. acid base
20. Identify the product for each step in the following reaction sequence. Write complete equations showing the structure of all reactants and products for each step. (a) Isopropyl benzene + NBS/heat ---------->A (b) A+ t-BuOK ---------> B (c) B + 1)BH3 followed by 2)H2O2/NaOH -----> C (d) C + PCC ------> D
How would you synthesize the following fatty acid from the organic building blocks and reagents in the following tables?Specify the building block (by number) first.Specify reagents in order of use (by letter) second.Example: 2be
Identify the organic functional groups and reaction type for the following reaction.Please include everything including the letter and the answers.The reactant is a(n)a. amideb. aldehydec. alcohold. carboxylic acide. esterf. ketoneThe product is a(n)a. carboxlyate ionb. ammonium ionc. alcohold. carboxylic acide. ketonef. aldehydeThe reaction type isa. hydrationb. esterificationc. hydrolysis (in acid)d. hydrolysis (in base)e. amide synthesisf. amide synthesisg. dehydrationh. acid base
The structure of limonene appears in Problem 25-13. Predict the products formed when limonene reacts with the followingreagents.(a) excess HBr (b) excess HBr, peroxides (c) excess Br2 in CCl4(d) ozone, followed by dimethyl sulfide (e) warm, concentrated KMnO4 (f) BH3 # THF, followed bybasic H2O2
When some sugars dissolve in water they spontaneously undergo changes in optical rotation called mutarrotation. The Mutarrotation of D-glucopyranose is catalyzed by acid and bases. 2-Hydroxypyridine is a more effective catalyst than phenol and pyridine for this reaction because: a.Both oxygen and N in 2-hydroxypyridine act as bases increasing the rapid interconversion of sugar b. The OH of 2-hydroxypyridine serves as the base while the current N as the acid. c. 2-hydroxypyridine acts both as a base to remove the proton from the hydroxyl group in the hemiacetal and as an acid to provide a proton to the oxygen in the hemiacetal. d.Phenol and pyridine are very expensive.
Stearidonic acid (C18H28O2) is an unsaturated fatty acid obtained from oils isolated from hemp and blackcurrant (see also Problem 10.11).a.What fatty acid is formed when stearidonic acid is hydrogenated with excess H2 and a Pd catalyst? b.What fatty acids are formed when stearidonic acid is hydrogenated with one equivalent of H2 and a Pd catalyst? c. Draw the structure of a possible product formed when stearidonic acid is hydrogenated with one equivalent of H2 and a Pd catalyst, and one double bond is isomerized to a trans isomer. d.How do the melting points of the following fatty acids compare: stearidonic acid; one of the products formed in part (b); the product drawn in part (c)?
Can 4-methylcyclohexanoic acid be reduced by NABH4?
The carbonyl group on D-glucose can be reduced to d-glucitol. Identify the reagents that can chrry out this reduction. A.water in acidic solution B. hydrogen with a Platinum catalyst (Hy/Pt) C. Sodium dichromate (NaCr2O) in acidic solution D. Benedict’s reagent E. Enzymes