After mechanism of this Reaction formed gylcerol and 3 molecules of CH3(CH2)12COONa
Hence correct answer is
Third option
What statement is TRUE about the mechanism for the reaction shown here? CH(CH) COACH CHỊ(CH3CO,CH NaOH...
What statement is TRUE about the mechanism for the reaction shown here? CHỊ(CH4)2COẠCH, CH,(CHỊ) CO,CH 2, CO,CH NAOH excess heat CHỊ(CH) CÓ CH, Water attacks the carbonyl carbon to form a tetrahedral intermediate. The first step of the reaction involves protonation of the ester carbonyl oxygen. One of the products formed is CH3(CH2)2CO2Na. Water deprotonates the alpha carbon.
What statement is TRUE about the mechanism for the reaction shown here? CH(CH2)2CO CH -COẠCH NaOH CH3(CH)1200CH excess heat CH(CH3COACH Water attacks the carbonyl carbon to form a tetrahedral intermediate. The first step of the reaction involves protonation of the ester carbonyl oxygen. One of the products formed is glycerol. The hydroxide deprotonates the alpha carbon. Which bases among the following is/are used for irreversible enolate formation of acetaldehyde? NaH NaOMe II LDA III NaNH2 IV NaOH y II and...
What statement is TRUE about the mechanism for the reaction shown here? CH;(CH)2CO,CH CH;(CH)2CO,CH „CO.CH NaOH CH;(CH)12CO,CH excess heat One of the products formed is ethylene glycol. The hydroxide deprotonates the alpha carbon. The first step of the reaction involves protonation of the ester carbonyl oxygen. The hydroxide attacks the carbonyl carbon to form a tetrahedral intermediate.
What product is expected from the tollowmg reaction но 1. LiAH cther 2. Но Оно ОН ОН ОН но ОН What statement is TRUE about the mechanism for the reaction shown here? CH,(CH2)2CO,CH CH3(CH)12CO,CH „Coch! NaOH excess heat CH3(CH)2CO,CH, Water attacks the carbonyl carbon to form a tetrahedral intermediate. The first step of the reaction involves protonation of the ester carbonyl oxygen. One of the products formed is glycerol. The hydroxide deprotonates the alpha carbon.
What is the IUPAC name of the given molecule? OH Br 1-bromo-2-ethyl-2-hydroxy-3-methylpentanoic acid 2-ethyl-3-methylpentan-2-ol-1-carboxyl bromide 2-ethyl-3-methyl-2-ol-pentanoyl bromide O2-ethyl-2-hydroxy-3-methylpentanoyl bromide What statement is TRUE about the mechanism for the reaction shown here? CH,(CH)2CO,CH, NaOH CH3(CH12COCH excess heat CH3(CH)2CO,CH2 Water attacks the carbonyl carbon to form a tetrahedral intermediate. The first step of the reaction involves protonation of the ester carbonyl oxygen. One of the products formed is glycerol. The hydroxide deprotonates the alpha carbon. Which bases among the following is/are used...
Choose the correct starting materials for the following Diels-Alder product: A CHO CHO CHO CHO CHO Doc CHO CHO CHO CHO 2.1 CHO Question 10(4 points) Which one of these compounds is insoluble in water, but soluble in both NaHCO3(aq) and NaOH(aq)? Ophenol O octanal O propanoic acid Op-methylbenzoic acid The best way to synthesize the following amine is: NH 2 H, N 1. NBS, bv 2. NaNH NHI O 1. NACN 2. LAIH 3. H,0 1. H.00 2. ex...
84. What two products are formed in the hydrolysis reaction shown below? heat CH-C-NHCHCH, + NaOH 0 CH, —C—OH A) + NHẠCH CHI B) CH3 -C-NH2 + Na+ "CH,CH; L. C) CH-C-NH, + CH,CH 0 D) CH,-0-0- Nat + NH CHỊCH __ + CH3-C-NH E) HOCH.CH
СО cat. H + NH2CH3 + H2CO2C CO2CH3 CO CHE Cocaine has been prepared by a sequence beginning with a Mannich reaction between dimethyl acetonedicarboxylate, methylamine, and butanedial. The mechanism involves the following steps: 1. Following initial protonation of the carbonyl oxygen, nucleophilic attack by the amine forms carbinolamine 1; 2. Proton transfer and elimination of water forms iminium ion 2; he enol form of the dicarboxylate ester attacks the iminium ion to form adduct 3; 4. Adduct 3 tautomerizes...
What two products are formed in the hydrolysis reaction shown below? heat CH,-C-NHCH,CH, + NaOH CHCOH NH,CH CH CHCNH2Na CH2CH O Na CH3CNaNH2CH CH CH, NHHOCH-CH
1.Provide the major organic product of the reaction below. 2.Provide the major organic product of the reaction shown below. 3.Provide the major organic product of the reaction shown below. 4.Predict the necessary starting material for the reaction below. Give the IUPAC name. 5. Part A Draw the carbonyl compound needed for this synthesis. 6.Predict the product formed when CH3-CH2-C≡C:–Na+ undergoes a reaction with the compound shown below followed by an aqueous workup.. Interactive 3D display mode 7. When 2,2-dibromo-1-phenylpropane is...