1. Hydration of acetaldehyde under acidic condition is shown in the figure below. The first step is protonation of the carbonyl oxygen with H+ of acid to generate a more electrophilic carbon. The water then attacks nucleophilically onto the electrophilic carbonyl carbon. Loss of an H+ to compensate the +ve charge developed on oxygen gives us the product.
2. Hydration of acetaldehyde under basic condition is shown below. The first step is attack of OH- onto the carbonyl carbon to generate a -vely charged Oxygen. The oxygen then picks up a proon from H2O in the system to yield the product as shon below.
Figure showing mechanism of hydration of acetaldehyde under 1. acidic and 2. basic medium
1. Draw the step-wise mechanism for the hydration of acetaldehyde under acidic conditions 2. Draw the...
Hydration of alkenes under aqueous acidic conditions. Draw the detailed stepwise mechanism for this reaction. Be sure to show all steps, intermediates, formal charges, and show the movement of electrons with curved arrows. You do not need to draw transition states. H2SO4 H20 ?? The hydration of alkynes can also occur under aqueous acidic conditions however, instead of forming the alcohol, a ketone is formed. Draw the detailed stepwise mechanism for the conversion of the alkyne to the ketone (one...
1 pt 1 pt The final step in the hydration of an alkyne under acidic conditions is the automerization of an enol intermediate to give the corresponding ketone. The mechanism involves a protonation followed by deprotonation Consider the following tautomerization reaction: CH2 CHE H,09 1 pt 1 pt 1 pt OH 1 pt 1pl For the mechanism step below, draw curved arrows to show electron reorganization Where relevant, a pi bond has two hot spots when you draw a curved...
10 pts: Draw the mechanism for the aldol condensation of two butanone molecules under acidic conditions.
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...
A. Products and Mechanism 1. Draw a detailed step-wise mechanism using curved arrow notation for the following reaction: EtO E t 1. xs PhMgBr 2. HCI, H,0
2. Draw the structures in the lettered boxes. ."Draw a step-wise arrow pushing mechanism for E and F NaH (1eq) CHJ но
Draw a mechanism for an esterification reaction between phthalic anhydride and ethylene glycol under acidic conditions. (I need help seeing how this reaction would occur with a molecule such as phthalic anhydride, thanks!)
show a mechanism of formatiin if the following enol under base catalyzed conditions We were unable to transcribe this imageShow a mechanism of formation of the following enol under base-catalyzed conditions: For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do n use abbreviations such as Me or Ph. Step 1 0 Get help answering Molecular Drawing question Draw step 1 of...
What would the mechanism for this E2 reaction be under acidic conditions? --PlayPosit 33: Ch OS & 09 X PlayPosit Interactive Video Player X ACE Question answering page e epochuky.edu/ace/homework/answerframejsp?prevMode=0¤tNum=17&showClock-false Erganic My Courses My Prod Course Home Assignments Grade Book Assignment 11: Drawing elimination products and mechanism Mammallowed Wies per question Unlimited H: (17) Draw a reasonable mechanism for this reaction. Al compounds involved in each stage of the mechanism must be enclosed in a bex, and each box must...
draw a step-wise mechanism for the reaction of 2- methyl-2-butanol with hydrochloric acid, which includes transition states.