Fischer esterification reaction. Because the alcohol oxygen is a poor nucleophile, the carbonyl carbon is made a better electrophile by protonation of the carbonyl oxygen. The steps of the synthesis are all reversible. The reaction is generally driven to completion by using an excess of the liquid alcohol as a solvent, or by distilling off the product as it forms. Draw curved arrows to show the movement of electrons in this step of the mechanism.
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Chemistry, 22.06.2019 14:30, joejoefofana
Consider the reduction reactions and their equilibrium constants. cu+(aq)+e−↽−−⇀cu(s)pb2+(aq)+2e−↽−−⇀ pb(s)fe3+(aq)+3e−↽−−⇀fe(=6.2×108=4. 0×10−5=9.3×10−3 cu + ( aq ) + e − ↽ − − ⇀ cu ( s ) k =6.2× 10 8 pb 2 + ( aq ) +2 e − ↽ − − ⇀ pb ( s ) k =4.0× 10 − 5 fe 3 + ( aq ) +3 e − ↽ − − ⇀ fe ( s ) k =9.3× 10 − 3 arrange these ions from strongest to weakest oxidizing agent.
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Chemistry, 23.06.2019 00:30, danielmartinez024m
Maya wrote if you step to describe how carbon circulates between the atmosphere and living organisms
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Chemistry, 23.06.2019 01:00, aliviadushane
If a straight-chain hydrocarbon is a gas at room temperature, how many carbon atoms will it have? a. 6 carbon atoms b. 12 carbon atoms c. 24 carbon atoms d. 3 carbon atoms
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Fischer esterification reaction. Because the alcohol oxygen is a poor nucleophile, the carbonyl carb...
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