(a)
Interpretation:
The structure of thioester formed when reaction takes place between
Concept Introduction:
Thioesters are prepared by condensation of carboxylic acid with a thiol. A molecule of water is lost on this reaction. The reaction that takes place in producing thioesters is known as thioesterification reaction.
Thioesterification reaction is the one in which the carboxylic acid is condensed with a thiol in presence of strong acid catalyst to produce thioester. The general reaction scheme can be given as,
(b)
Interpretation:
The structure of thioester formed when reaction takes place between carboxylic acid given and the thiol given has to be drawn.
Concept Introduction:
Thioesters are prepared by condensation of carboxylic acid with a thiol. A molecule of water is lost on this reaction. The reaction that takes place in producing thioesters is known as thioesterification reaction.
Thioesterification reaction is the one in which the carboxylic acid is condensed with a thiol in presence of strong acid catalyst to produce thioester. The general reaction scheme can be given as,
(c)
Interpretation:
The structure of thioester formed when reaction takes place between carboxylic acid given and the thiol given has to be drawn.
Concept Introduction:
Thioesters are prepared by condensation of carboxylic acid with a thiol. A molecule of water is lost on this reaction. The reaction that takes place in producing thioesters is known as thioesterification reaction.
Thioesterification reaction is the one in which the carboxylic acid is condensed with a thiol in presence of strong acid catalyst to produce thioester. The general reaction scheme can be given as,
(d)
Interpretation:
The structure of thioester formed when reaction takes place between carboxylic acid given and the thiol given has to be drawn.
Concept Introduction:
Thioesters are prepared by condensation of carboxylic acid with a thiol. A molecule of water is lost on this reaction. The reaction that takes place in producing thioesters is known as thioesterification reaction.
Thioesterification reaction is the one in which the carboxylic acid is condensed with a thiol in presence of strong acid catalyst to produce thioester. The general reaction scheme can be given as,
Want to see the full answer?
Check out a sample textbook solutionChapter 16 Solutions
Study Guide with Selected Solutions for Stoker's General, Organic, and Biological Chemistry, 7th
- 4. Redraw the following compounds from most reduced to most oxidized. If compounds have identical oxidation states, draw them under each other. OH میر محمد ملک OH OH .OH OH HS سلام پر من OH most reduced most oxidizedarrow_forwardPlease correct answer and don't used hand raitingarrow_forwardAfter 2-Bromo-3,3-dimethylbutane was reacted with KOC(CH3)3 a 1H NMR spectrum was obtained of the product. Propose a structure for the product of this reaction.arrow_forward
- 3. The compound 5-hydroxymethyl furfural forms while heating or cooking sugar-containing foods. དང།།སྤུ་ -OH OH 5 hydroxymethyl furfural a. Draw arrow-pushing mechanism for the dehydration of fructose under acidic conditions (use H-A). b. What is the driving force for this reaction?arrow_forward2. Consider the following reaction OH + PPO OH a. Draw the resonance structures of the intermediate that is formed after the benzene ring reacts with the allylic carbocation. b. Provide arrow-pushing mechanism for the formation of the product from the intermediate formed in part a.arrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts. OH (CH3CH2)3SICI, EtзN Drawingarrow_forward
- 5. Provide arrow-pushing mechanism for the following isomerization reaction но аб. Но + быarrow_forwardPlease correct answer and don't used hand raitingarrow_forward4. Unsaturated fatty acids are fatty acids that contain one or more double bonds. Double bonds can form by dehydration reaction as demonstrated below. Propose a one-step mechanism for an enzymatic dehydration reaction using histidine and aspartic acid side chains. H OH O ACP `ACParrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning