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 carboxylic acid by methoxide ion.
(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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- 2 3 5 [Review Topics] Reagents HBr a. b. C. H₂O, H₂SO4 d. Br₂ Cl₂ H₂, Pd Br₂, H₂O Cl₂, H₂O OsO4 then NaHSO3 e. f. g. h. i. j. k. I. [References] HBr, H₂O2, hv Hg(OAc)2, H₂O then NaBH4 BH3 then H₂O2, NaOH O3 then (CH3)2S m. n. O. p. q. r. S. t. u. V. 2 equivalents of NaNH₂ H₂, Lindlar's catalyst Na/NH3 H₂SO4, HgSO4 (sia)2BH then H₂O₂, NaOH 1 equivalent of NaNH2 NBS, hv Br₂, hv Cl₂, hv HCI Identify the reagents necessary to accomplish the following steps in the above synthesis of 3-hexanone from acetylene: Step 4: v Step 5: F Step 7: Previous Next Save and Exitarrow_forwardnurbuks alixir 9 and lead). solution of ammonium chloride ) (~Hyl) acetate (Pb(CH3006) ₂ This solid? produces a solid. What is the identity of Bott A. Pb (CH₂COO), B. Pb (NH4)₂ C. (NH4), 4 D) Pb C (W) J Ẹ NH, CH, Coo Expl 49 42-0 CO C-PF St LGO (23 21 HO SA R الموت id boke slit + CXIC moth SHMOB stata Garrow_forwardBelow is the structure of terbutaline, used in the management of asthma symptoms. The tert-butyl substituent on the Nitrogen provides .?. selectivity. OH TERBUTALINE HO ÓH Select one: a.Muscarinic b.Nicotinic c.B1-adrenergic d.al-adrenergic e.82-adrenergicarrow_forward
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- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning