Please explain your work and include a mechanism!!! Why would a methyl ester be a bad...
Please show work thanks Show how to accomplish the following transformation. Your answer must include a Grignard reaction and the use of a protecting group. (15 point OH OH Br OH
2) Amines are often protected with the tert-butyloxycarbonyl BOC) group. Show the mechanism of fomation of the BOC protected amine (a carbamate). Be sure to show all bonds formed broken and inclade all intermediates including the appropriate formal charge BOOO Do you expect that the carbamate functional group is more or less reactive than an amide towards nacleophilic addition? Bricfly explain your reasoning The BOC protecting group can be removed under acidic conditions, such as treatment with tnifloroacetic acid (TFA)...
Draw the reaction mechanism for the nitration of methyl benzoate to methyl nitrobenzoate, please show all resonance structures for each possible substitution position to explain why methyl m-nitrobenzoate was the favored isomer.
Write the mechanism for the formation of Malachite Green from methyl benzoate. Be sure to show all steps, including the loss of water. 1. 2. Write the mechanism for the formation of Crystal violet from diethyl carbonate. 3. Methyl benzoate is an ester, but is technically a carboxylate ester. Diethyl carbonate is a 4. Why is the green dye in this experiment called "Malachite Green"? Hint: Try looking in a 5. Write the balanced equation for the reaction of hydrochloric...
What is the mechanism for base-catalyzed transesterification with methanol where the ester reacts with an alcohol solvent to form a new ester that contains the alcohol's OR group? Please draw out mechanism and explain. the reaction will use the reagents XS NaOCH3 (from NaOH, CH3OH) to convert vegatable oil (a fatty acid triester) to glycerol and 3 moles of methyl oleate (biodiesel)
Please explain this mechanism and why the ester is used as the electrophile rather than the ketone. + = 0 1) NaOCHZ CH2OH 2) H3O+ workup
1. a. Please draw the scheme for epoxidation of alpha methyl styrene with mCPBA. Include arrows and charges. 1. b. Please draw the reaction mechanism for the epoxidation of mCPBA with alpha methyl styrene. Include arrows and charges.
can you please show the work.. thank you in Black New Tab MyUn Sign in Learn @ cheggc GetH Mic x Sign .pdf 1) Choose one molecule from the set and create an 8-step synthesis scheme using the chosen molecule as your starting material. You need to write the complete set of reagents and draw the product expected from each step. Reagents typically used together are considered one step, e.g. 1) LAH 2) H20 should be considered as one step....
Please solve this. Include show work and explain the reasoning. Thank you! Four points are labeled on a graph. Rank the slopes of the graph at the labeled points. Explain your reasoning.
Banana oil, AKA isopentyl acetate, contains the ester functional group (like methyl benzoate). What products are formed if isopentyl acetate is treated with a huge excess of water in the presence of a dilute acid catalyst? Briefly explain. You will need to look up the structure of isopentyl acetate. Your answer should include a balanced reaction