please draw the structure needed. thank you
The alcohol oxygen attacks at the carbon containing the OTs leaving group. OTs leaves and a new C-O bond is formed in the Williamson's ester synthesis. the product structure is shown below.
please draw the structure needed. thank you The p -toluenesulfonate shown undergoes an intramolecular Williamson reaction...
The following molecule undergoes an intramolecular reaction in the presence of pyrrolidinium acetate. Draw the compound formed from dehydration of the product shown below. The following molecule undergoes an intramolecular reaction in the presence of pyrrolidinium acetate. Draw the compound formed from dehydration of the product shown below. Me Me NAcO Me Me HO HO Me Me Me Me Me Me HO Me . Draw all enolates in their carbanion form . You do not have to consider stereochemistry
draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOH3. Indicate the stereochemistry of the product. explanations are highly appreciated. thank you. (please show answer with dash and wedge) Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NAOCH3. Indicate the stereochemistry of the product Interactive 3D display mode CH3 CH3 Н.С" Br ШИ
Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOCH3. Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOCH3. Indicate the stereochemistry of the product.
draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOH3.Indicate the stereochemistry of the product.
Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOCH3. Indicate the stereochemistry of the product. Interactive 3D display mode
Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOCH3. Indicate the stereochemistry of the product. Interactive 3D display mode H2C.
Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOCH3. Indicate the stereochemistry of the product Interactive 3D display mode CH, ||llo _CH3 Ho B
Draw the organic product formed when the structure shown below undergoes a reaction with CH3C?CNa. Draw the organic product formed when the structure shown below undergoes a reaction with CH3C?CNa.
a) Draw the mechanism (with curved arrows) for the reaction of the conjugate base of p?hydroxybenzaldehyde with methyl p?toluenesulfonate. b) What ether would you obtain from the reaction of CH3CH2O- with 1?iodopentane? Draw the structure of the product. c) Explain in general how TBAS (Bu4N+HSO4-) works as a phase transfer catalyst in this reaction. What anion does Bu4N+ shuttle into the organic layer? d) p-Hydroxybenzaldehyde has four signals in the NMR, with the following chemical shifts and multiplicities. Assign each...
Predicting Products: Draw the structure of the one major organic product of each reaction in the boxes provided. Be aware that the products all have the molecular formula C6H100, but oth products are constitutional isomers of one another. Stereochemistry should be shown if applicable. HO. Nah, DMSO Br HO, Nah, DMSO Br An efficient way to prepare asymmetrical ethers was developed by a British scientist, Alexander Williamson. Show what reagents you would use to prepare the following compound via a...