Concept explainers
(a)
To determine: The product obtained from the reaction of triolein with
Interpretation: The product obtained from the reaction of triolein with
Concept introduction: The mixture of sodium hydroxide (Strong base) and water is used to convert ester into an ester salt of metallic sodium. The mechanism of the reaction comprises three steps. The first step is the addition of nucleophile. The second step is elimination of the leaving group. The third step is the deprotonation of
(b)
To determine: The product obtained from the reaction of triolein with
Interpretation: The product obtained from the reaction of triolein with
Concept introduction: Hydrogen gas in the presence of metal catalyst is used to reduce
(c)
To determine: The product obtained from the reaction of triolein with
Interpretation: The product obtained from the reaction of triolein with
Concept introduction: The reaction of an
(d)
To determine: The product obtained from the reaction of triolein with ozone and then dimethyl sulphide.
Interpretation: The product obtained from the reaction of triolein ozone and then dimethyl sulphide is to be stated.
Concept introduction: Ozonolysis is the oxidative cleavage of the double bond, where
(e)
To determine: The product obtained from the reaction of triolein with warm
Interpretation: The product obtained from the reaction of triolein with warm
Concept introduction: Potassium permanganate is a strong oxidising agent. In hot water it cleaves unsaturated hydrocarbon and convert it into acid.
(f)
To determine: The product obtained from the reaction of triolein with
Interpretation: The product obtained from the reaction of triolein with
Concept introduction: Simmons-smith reactions are those in which methylene iodide reacts with zinc-copper to gives a carbenoid which is known as Simmons-smith reagent. This carbenoid reacts with an alkene to give cyclopropane product.

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Chapter 25 Solutions
Organic Chemistry Plus Masteringchemistry With Pearson Etext, Global Edition
- 5. Write the formation reaction of the following complex compounds from the following reactants: 6. AgNO₃ + K₂CrO₂ + NH₄OH → 7. HgNO₃ + excess KI → 8. Al(NO₃)₃ + excess NaOH →arrow_forwardIndicate whether the product formed in the reaction exhibits tautomerism. If so, draw the structure of the tautomers. CO₂C2H5 + CH3-NH-NH,arrow_forwardDraw the major product of this reaction N-(cyclohex-1-en-1-yl)-1-(pyrrolidino) reacts with CH2=CHCHO, heat, H3O+arrow_forward
- Draw the starting material that would be needed to make this product through an intramolecular Dieckmann reactionarrow_forwardDraw the major product of this reaction. Nitropropane reacts + pent-3-en-2-one reacts with NaOCH2CH3, CH3CHOHarrow_forwardIndicate whether the product formed in the reaction exhibits tautomerism. If so, draw the structure of the tautomers. OC2H5 + CoHs-NH-NH,arrow_forward
- Explain how substitutions at the 5-position of barbituric acid increase the compound's lipophilicity.arrow_forwardExplain how substitutions at the 5-position of phenobarbital increase the compound's lipophilicity.arrow_forwardName an interesting derivative of barbituric acid, describing its structure.arrow_forward
- Briefly describe the synthesis mechanism of barbituric acid from the condensation of urea with a β-diketone.arrow_forwardGiven the hydrazones indicated, draw the structures of the enamines that can be formed. Indicate the most stable enamine (explain). C6H5 C6H5 H C6H5 Harrow_forward4. Propose a Synthesis for the molecule below. You may use any starting materials containing 6 carbons or less (reagents that aren't incorporated into the final molecule such as PhзP do not count towards this total, and the starting material can have whatever non-carbon functional groups you want), and any of the reactions you have learned so far in organic chemistry I, II, and III. Your final answer should show each step separately, with intermediates and conditions clearly drawn.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
