Please show the mechanism with acid.
based on the product formation the reaction mechanism is
as follows
Please show the mechanism with acid. 2. Write the complete reaction mechanism for the KCN-catalyzed reaction....
Acid-catalyzed dehydration of 2,2-dimethylcyclohexanol yields 1,2-dimethylcyclohexene as one of the major products. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures. ОН CH: CH3
Can you check my answers please? To answer the questions below use the following information: Cyanohydrins are important intermediates in the synthesis of c-hydroxycarboxylic acids from ketones and aldehydes. The nitrile functional group can be hydrolyzed by aqueous acid to yield a carboxylic acid. Nitriles can also be hydrolyzed to carboxylic acids using aqueous base. Unfortunately, when a cyanohydrin is treated with aqueous base the original carbonyl compound is isolated OH CHCOOH HO CN OBU H HCEN H NAOH H20...
5. Consider the reaction below. Write the complete stepwise mechanism for the reaction shown above. Show all intermediate structures and all electron flow with arrows. но он base catalyst ant 6. Give the major organic product(s) for the following reactions or sequence of reactions. Show all relev stereochemistry. Answer only 5 parts. If you think reaction de a.
Acid-catalyzed dehydration of 2, 2-dimethylcyclohexanol yields 1, 2-dimethylcyclohexene as one of the major products. Write complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures Consider the Grignard reaction below to answer the following questions The electrophile in this reaction is: The nucleophile in this reaction is: The alcohol product can be classified as 1'' alcohol 2'' alcohol 3'' alcohol 4'' alcohol Write the mechanism for the above reaction
Write the complete step-wise arrow-pushing mechanism for reaction shown below. Show electron flow with arrows, and be sure to include all intermediate structures. You must be very detailed in your mechanism for full credit. HO -CH₂CH₃ CH2CH3 -CH2CH3 CH2CH3 H2SO4
Write the complete stepwise mechanism for the reaction below. Show all intermediate structures and all electron flow with arrows. Exhibit 23-2 Consider the reaction below to answer the following question(s): NaOEt EtOH + H2O
Use arrows to show correct electron flow in the mechanism for the reaction below. Include all intermediate structures correctly drawn with formal charges. 3) Use arrows to show correct electron flow in the mechanism for the reaction below. Include all intermediate structures correctly drawn with formal charges. но H30t, heat он
5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures. (10 Points) CH, Br2 Br (or Cla) HI Br 7 6. Predict the major product for the following reactions PhCOM
Could someone help me out on this problem. 1. Write the complete reaction mechanism for the following reaction. Show all electron flow with arrows and show all intermediate structures. NH2 H + 0.5-OO + H2O
Write the complete stepwise mechanism for the following reaction Show all intermediate structures and all electron flow with arrows. Draw the mechanism for the following reaction. Show stereochemistry for every step of the reaction.