subject
Chemistry, 04.04.2020 02:22 derekcalhoun4943

In the Fischer esterification reaction, a carboxylic acid reacts with an excess of alcohol in acidic conditions to form an ester. During the reaction the sp2 hybridized carbonyl carbon of the acid forms an sp3 hybridized intermediate before returning to sp2 hybridization in the product. Draw the structure of the neutral sp3 hybridized intermediate and the ester product in the reaction between pentanoic acid and n-propanol.

ansver
Answers: 1

Another question on Chemistry

question
Chemistry, 21.06.2019 17:40
If 10.0 ml of the solution on the right are withdrawn from the 100 ml beaker and diluted again in a similar manner, what is the new concentration? m nacl
Answers: 2
question
Chemistry, 21.06.2019 20:30
Which of the following pairs of elements belong to the same groupa. h and he b. li and bec. c and pb d. ga and ge
Answers: 1
question
Chemistry, 22.06.2019 03:30
Select the correct answer. when carbon dioxide dissolves in water, it sometimes reacts with water to form carbonic acid as in this balanced equation: co2 + h2o → h2co3. if 495 milliliters of carbon dioxide at 25°c and 101.3 kilopascals reacts with excess water, what is the theoretical yield of carbonic acid? use the periodic table and the ideal gas resource a. 0.889 g b. 1.10g c. 1.27g d. 2.02g what's the answer! quick!
Answers: 1
question
Chemistry, 22.06.2019 04:00
Electric charge is what ? a. kinetic energy b. radiation c. discovery d. electricity
Answers: 1
You know the right answer?
In the Fischer esterification reaction, a carboxylic acid reacts with an excess of alcohol in acidic...
Questions
question
Chemistry, 29.09.2019 02:10
Questions on the website: 13722367