ochem 2nd semseter o 6) Acid catalyzed transesterification is a convenient method to exchange the alkoxy...
1) Draw a rational mechanism for the reaction shown below. Use curved arrows appropriately. Show all relevant intermediate(s) and lone pairs of electrons and formal charges where appropriate. HO H2SO4 Ome
Write the complete stepwise mechanism for the acid catalyzed hydrolysis of the compound shown. Show all intermediates, indicate with curved arrows the movement of electrons and show all formal charges and lone pairs of electrons where relevant. Will rate and comment, thank you in advance!
Draw the mechanism for the reaction shown below: o This mechanism requires 6 distinct steps This is an acid-catalyzed reaction, use the H30+ in your mechanism o Be sure to include all curved arrows to show the movement of electrons Be sure to include all lone pairs and formal charges on atoms, as necessary For each step in your mechanism, label it based on the type of mechanism step it is H H :N-H
please help me solve both of these!! Write the complete stepwise mechanism for the acid catalyzed hydrolysis of the compound shown. Show all intermediates, indicate with curved arrows the movement of electrons and show all formal charges and lone pairs of electrons where relevant. Write the structure of the Michael addition product and the final Robinson annulation product when using the following starting materials. Hint: the dialdehyde is the Michael donor and the ketone is the Michael acceptor. Н Michael...
2) Draw a rational mechanism for the reaction shown below. Use curved arrows appropriately. Show all relevant intermediate(s) and lone pairs of electrons and formal charges where appropriate. Show ALL STEPS (i.e Reaction 2) 1) Na O Et, EtOH Et 2) H20, HCI Et
i really need help, please help i will rate thanks Write the complete stepwise mechanism for the acid catalyzed hydrolysis of the compound shown. Show all intermediates, indicate with curved arrows the movement of electrons and show all formal charges and lone pairs of electrons where relevant
The Claisen condensation converts 2 molecules of an ester into a B-keto ester. The reaction starts with the ester in an alkoxide/alcohol solution and is worked up with acid to form the neutral B-keto ester product. :0 O: 1. -OCH2CH3/CH3CH20H 2 2. H30 OH Show the curved-arrow mechanism for the Claisen condensation of ethyl ethanoate treated with ethoxide ion. Include all formal charges and nonbonding electrons. In each step, draw only the species that react in that step. If an...
QUESTION 1 Using the curved arrow formalism, outline an acceptable mechanism for the acid catalyzed electrophilic addition of water to 1-Methylcyclohexene as shown below. Your mechanism should show the movement of all electrons involved in bond forming and bond breaking steps as well as all formal charges for atoms that are not neutral CH, HO -H
2. (5 pts) Draw out the mechanism for the acid-catalyzed dehydration shown below. Include all steps, clearly show all charges, and all unshared electron pairs. Use curved arrows to show electron movement in all making and breaking of bonds. NOTE: To show the breaking of a bond you must draw the bond explicitly so that you can clearly draw an arrow from the electrons in the bond. : OH Q" - W H;0* -H;0
3. Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use curved arrows to indicate the flow of electrons. (Note: use hydronium ion, H307, in your mechanism to indicate "acidic water"). (6 pts) 4. Draw a stepwise, detailed mechanism for the reaction below. Use curved arrows to indicate the flow of electrons. (Hint: think of this reaction as a combination of addition of HX (step 1) and hydration (step 2)]. In the second step, an...