Question

In an esterification lab how is the remainder of the acetic acid removed? Include a chemical equation in your answer. Part of the slide below was cut off in the power point.

organic CH&COO phaseH20 (trac CH3COOR H2SO4 (trace) extract with NaHCO3 organic phaseCH3COOH (trace) extract with ROH CH3COOH

0 0
Add a comment Improve this question Transcribed image text
Answer #1

Everything I have explained in a neat and clean way with proper explanation, for all that you need to see just this attachment, hope you will love the solution/explanation like this, Thank you :) and have a good day ahead !!!

an eastenCaceho auid is some wd le- CH tafor traea trale amwt

Add a comment
Know the answer?
Add Answer to:
In an esterification lab how is the remainder of the acetic acid removed? Include a chemical...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • PREPARATION OF PHARMACEUTICALS - Fischer Esterification Reactions Q: Calculate the expected mass of both methyl salicylate and aspirin assuming 100% yield. EXPERIMENT7 PREPARATION OF PHARMACEUTICALS...

    PREPARATION OF PHARMACEUTICALS - Fischer Esterification Reactions Q: Calculate the expected mass of both methyl salicylate and aspirin assuming 100% yield. EXPERIMENT7 PREPARATION OF PHARMACEUTICALS Fischer Esterification Reactions Almost 2500 years ago, physicians such as Hippocrates recommended that patients chew on the bark of the willow to alleviate pain. The active ingredient in willow bark was found to be salicin, a compound made of a molecule of salicyl alcohol bonded to a p-D-glucose molecule. In the stomach, the bond between...

  • Working on the questions at the end of this lab report (see above). I need help answering questio...

    Working on the questions at the end of this lab report (see above). I need help answering questions 2, 3, and 4 completely and thoroughly. Thank you! s, until the I hexano 1 clean disti CYCLOHEXENE from CYCLOHEXANOL be dehydrated with solfuric acid to yield cyclohexene and waterf Add a 0°C (record ct and cal H,SO + H20 ainer. s in purification of any crude product are (a) the preliminary separation of the product from the reaction mixture by distillation...

  • Give a detailed mechanism for this reaction and give a separation scheme NUCLEOPHILIC ACYL SUBSTITUTION: Synthesis...

    Give a detailed mechanism for this reaction and give a separation scheme NUCLEOPHILIC ACYL SUBSTITUTION: Synthesis of an Ester Isoamyl acetate (Banana Oil) Purpose This experiment demonstrat and alcohol. The technique of refluxing the reaction mixture is introduced. es the procedure for the synthesis of an ester from a carboxylic acid Esters are an important functional group in organic chemistry, and esters are found widely distributed in nature. Many lower molecular weight esters are associated with natural fuit flavors and...

  • Attached is the lab experiment. Here are the questions I need help with: 1. What is...

    Attached is the lab experiment. Here are the questions I need help with: 1. What is the purpose of each of the following steps in this experiment? a. Adding solid NaCl to the reaction mixture b. Repeated washings with water, sat'd NAHCO3, and brine c. the pipet column chromatography 2. Which compound, cyclohexanol or cyclohexanone will have a higher Rf on a TLC plate? 3. What is the advantage of using sodium hypochlorite as an oxidant over CrO3 or Na2Cr2O7...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT