a) 5 member ring formation is more favourable than 7 member ring. So 7 member ring is the least likely to be formed.
b) By abstracting alpha H next to keto and aldehyde 5 member ring is formed. But abstraction of aldehydic alpha H is more easier than abstracting alpha H of keto. So the last product is major which is formed by abstraction of aldehydic alpha H.
7. Under the following conditions, three products are formed in this reaction. OH H2O a. Draw...
(6) Draw the structures of the three elimination products formed in this reaction. Circle the most stable product formed. Is this mechanism of type E1 or E2? H3PO4 OH heat
Draw the three organic products formed from the following reaction with excess acid and water. H2O NH O Draw two monomers that could produce the following polymer. Dext Draw an ester and a Grignard reagent that would make the following compound. OH fo
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. mer 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. H3C CI CH OH CH2CH3 општироотип солио 3. Provide the product/s for the following reactions. Indicate if the reactions proceed via an SN1, or SN2 mechanism. Indicate proper stereochemistry if it is applicable. Show the mechanisms NaCN...
Draw ALL possible unimolecular elimination (E1) products formed under the reaction conditions below; don't worry about specifving the maior vs, minor products. Where relevant, indicate the stereochemical outcome. 1. OTf E1OH 70 °C
4. Propose a mechanism for the formation of the following products OH +OH Br 5. Draw the structure of product formed in the following reaction Cl C4HgS Na DMSO Cl Draw the mechanism leading to product formation.
2. A reaction discussed in class involved treating a primary amine with chloroform under basic! conditions to form an isocyanide. When a secondary amine was used instead, an amide was formed: NaOH NaOH CHCIE R-NEC + CHCIE RNH2 + Lº amine RỌNH 2° amine HANR2 2. A reaction discussed in class involved treating a primary amine with chloroform under basic conditions to form an isocyanide. When a secondary amine was used instead, an amide was formed: NaOH NaOH CHCIE R-NEC...
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. BEBE 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. HyCc CH OH CH CHE
Establish what is the starting material(s) for the reaction and draw a full mechanism for the following reactions: Establish what is(are) the starting material (s) for the reactions, and draw a full mechanism for the ing reaction. a) NaOH, H2O, HEAT b) work-up Draw a mechanism that explains the formation of the product under the given reaction conditions a) NaOH, H2O b) work-up OH Establish what is(are) the starting material (s) for the reactions, and draw a full mechanism for...
1. Draw a mechanism for the following Aldol condensation reaction under basic conditions, including the formation of the enolate. Please include ALL lone pair electrons, formal charges, and stereo/regiochemistry whenever applicable. 1) LDA, H2O 2) LAH 2. Draw a mechanism for the following Dieckmann reaction under basic conditions, including the formation of the enolate. Please include ALL lone pair electrons, formal charges, and stereo/regiochemistry whenever applicable. 1) NaOEt 2) Hзо* OEt 3. Draw a mechanism for the following alkylation reaction...
Draw the organic products formed in the following reaction. OH HO heat