Question

During the experiment, what happened to the other enantiomer of phenylsuccinic acid? How could you isolate...

During the experiment, what happened to the other enantiomer of phenylsuccinic acid? How could you isolate (R) – phenylsuccinic acid. Write out a clear, detailed experimental procedure to isolate the (R) enantiomer from today’s experiment.

Homework Answers

Answer #1

Recovery of (R)-(-)- phenylsuccinic acid-

Other enantiomer i.e. (R)-(-)-phenylsuccinic acid, is dissolved in solvent. This solvent is evaporated at the rotary evaporator. Solid material is obtained which is enriched with (R)-(-)-enantiomer. Add 15 mL of cold 6M HCl to the solid residue in the recovery flask. Scrape down the sides of the recovery flask, and stir the reaction mixture for 10-15 minutes. Filter the solid product using vacuum. Rinse the recovery flask with 15 mL of cold water and filter to recover the remaining solid. Wash the solid residue on the filter paper with 15 mL of cold water. Dry the solid for 10-15 minutes. This solid is enriched (R)-(-)-phenylsuccinic acid.

Know the answer?
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
Similar Questions
During the experiment, what happened to the other enantiomer of phenylsuccinic acid? How could you isolate...
During the experiment, what happened to the other enantiomer of phenylsuccinic acid? How could you isolate (R) phenylsuccnic acid. Write out a clear, detailed experimental procedure to isolate the (R) enantiomer from today's experiment (using (R)-proline is not an option!)  
Tuskegee experiment. Most people's initial reaction to the Tuskegee experiment is to ask how it could...
Tuskegee experiment. Most people's initial reaction to the Tuskegee experiment is to ask how it could have happened? What do you think? Given today’s laws of informed consent, could it happen again? Why do you feel that way? How does the Tuskegee study differ from today’s research studies for HIV and AIDS?
You have a protein with a sulfhydryl group (S-H) how could you use that to isolate...
You have a protein with a sulfhydryl group (S-H) how could you use that to isolate your protein? Another option would be to use a 6X histidine linker. How would that work? Would one have an advantage over the other?
In a chemistry experiment in which you extract and isolate caffeine from tea leaves...what is the...
In a chemistry experiment in which you extract and isolate caffeine from tea leaves...what is the mobile and stationary phase?
Question must be solved using only symbolic algebra. During the experiment if you could triple the...
Question must be solved using only symbolic algebra. During the experiment if you could triple the breakaway magnetic force with all other quantities left unchanged, what is the new value for the critical velocity if it was v0 (initial velocity), initially? (b) Now if you halved the radius with all other quantities left unchanged, what is the new critical velocity if it was v0 (initial velocity), initially? (c) If during the experiment, critical velocity quadrupled with all other quantities left...
We performed a bromination of trans-stilbene in lab (A green chemistry experiment). Suppose that you perform...
We performed a bromination of trans-stilbene in lab (A green chemistry experiment). Suppose that you perform the same reaction under different conditions (in which a different mechanism operates), and you end up with a product that is a mixture of (R,S), (R,R), and (S,S). Which purification technique could be used to isolate the (R,S) compound from the other two stereoisomers? Explain why this technique would be successful. Why can the (R,S) isomer be separated from the other two? Explain your...
Write a procedure so a lab mate could prepare 100 mL of buffer solution of that...
Write a procedure so a lab mate could prepare 100 mL of buffer solution of that pH from two solids. Your procedure should clearly indentify which glassware and chemicals you will use to prepare the solution. Assume that you will use the sodium salt of the conjugate base to prepare the solution. Our desired pH is 7.5 and the weak acid I chose is Sodium hydrogen sulfite with pKa of 7.21. Use Henderson-Hasselbalch equation to determine molequantities of the weak...
1) How would your process for Part A have beeen different if you had used sulfuric...
1) How would your process for Part A have beeen different if you had used sulfuric acid in this experiment instead of hydrochloric acid? Be specific. (Hint: write out the balanced equation for the reaction between sulfuric acid and NaOH and discuss titration analysis.) 2) How would your results be affected if you forgot to "clear the jet" of the buret before proceeding with your titration? Be specific. 3) During the analysis, you periodically washed odwn the sides of the...
In this experiment a racemic mixture of a diamine called trans-1,2-diaminocyclohexane (basic substances) was converted to...
In this experiment a racemic mixture of a diamine called trans-1,2-diaminocyclohexane (basic substances) was converted to a diastereomeric salt mixture using optically pure L-(+)-tartaric acid. This salt mixture will be separated using crystallization techniques. The salt from the (R,R) diamine was less soluble than the salt from the (S,S) diamine and was separated by a vacuum filtration. How could you convert your salt back to the free diamine? Describe the experimental details that would be needed to regenerate your optically...
Part 1: Imagine that you were a participant in an experiment where you were asked to...
Part 1: Imagine that you were a participant in an experiment where you were asked to eat cookies and rate how much you liked each cookie on a scale from 1 to 5, where higher ratings mean higher liking of the cookie. You are asked to eat an Oreo cookie and rate it and then eat a Chips Ahoy cookie and rate it. For this experiment, answer the questions below. . What are some of the potential biases in this...