Question

Organic chemistry help?

2. Eight grams of compound Y was recrystallized us

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

m = 8 g of Y

V = 103 mL

S = 8/103 = 0.077669 g /mL at T = 100°C

for the second crystallisation:

50 mL --> 0.077669*50 = 3.88345 g of salt should be in solution

then, after crystallisation,

0.957*3.88345 = 3.7164 g were recovered, meaning that

3.88345 -3.7164 = 0.16705 g are in solution

so

S2 = mass/V = 0.16705/50 = 0.003341 g /mL

Solubility at 100°C -->  0.077669 g /mL

Solubility at 20°C --> 0.003341 g /mL

Add a comment
Know the answer?
Add Answer to:
Organic chemistry help? 2. Eight grams of compound Y was recrystallized using the minimal amount of...
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
  • This is a post-lab question of the Recrystallization of Aspirin experiment. This is related to organic...

    This is a post-lab question of the Recrystallization of Aspirin experiment. This is related to organic chemistry. Please be detailed, thank you! Given the table for solubility of compounds X and Y in solvent Z. If 2.00 grams of impure compound X (contaminated by 12.0% Y by weight) is recrystallized from 25.0mL of solvent Z, what will be the purity of recrystallized X? Solubility per 100 g of Solvent Z Compound 20℃ 80℃ X 1.0 g 8.0 g Y 0.70...

  • 1. Compound X has a solubility in toluene of 18 mg per 100 mL at 20...

     1. Compound X has a solubility in toluene of 18 mg per 100 mL at 20 °C, and a solubility of 0.64 g per 100 mL at 70 °C. You are given a sample of 0.48 g of compound X which is contaminated with 25 mg of compound Y. A. If compound Y is always soluble in toluene, describe in detail how you could separate Y from X. Would x now be pure? B. If compound Y has approximately the same values of...

  • Multistep Synthesis: Synthesis of Amine (Organic Chemistry Lab) Question 1. Explain each step of reaction mechanism....

    Multistep Synthesis: Synthesis of Amine (Organic Chemistry Lab) Question 1. Explain each step of reaction mechanism. (How does it work?) 2. Discuss reason for reaction sequence. (Why must one reaction occur before another?) 3. Explain how IR supports the major product. Experiment Procedure Imine Formation: Weigh a 20 mL beaker and then add 380 mg of ortho-vanillin and 268 mg of para-toluidine. Care should be taken to add equivalent molar amounts of the two reactants. Observe the mixture and record...

  • Principles of Inorganic Chemistry! Week 5 Effect of Temperature on Solubility of a Salt In this experiment, you w...

    Principles of Inorganic Chemistry! Week 5 Effect of Temperature on Solubility of a Salt In this experiment, you will study the effect of changing temperature on the amount of solute that will dissolve in a given amount of water. Water solubility is an important physical property in chemistry, and is often expressed as the mass of solute that dissolves in 100 g of water at a certain temperature. In this experiment, you will completely dissolve different quantities of potassium nitrate,...

  • please answer all parts I am trying to check my answers. Recrystallization of Acetanilide Recrystallization is...

    please answer all parts I am trying to check my answers. Recrystallization of Acetanilide Recrystallization is an important method used by chemists to purify solid compounds. When a chemist conducts a chemical reaction as shown in Scheme 1, it will rarely go to 100% completion, and will frequently produce byproducts. These byproducts and some of the unreacted starting materials will be present in the end as impurities. Chemists need ways to remove these unwanted impurities so they can isolate their...

  • Need help on providing reactions that describe the acid-base extraction and neutralization processes used in this exper...

    Need help on providing reactions that describe the acid-base extraction and neutralization processes used in this experiment. Provide a statement of solubility of each starting material and product. The experiment to be performed this week involves liquid-liquid extraction using a separatory funnel. Read chapter 15 in Zubrick to familiarize yourself with the use of the glassware for extraction and washing. Acid/Base Extraction Liquid-liquid extraction is a technique that can be used to physically separate two substances that have varying solubility...

  • need help answering these questions Chemistry 2211(PRIVATE) LABORATORY PRACTICUM - 4 DO NOT CONSULT WITH OTHER...

    need help answering these questions Chemistry 2211(PRIVATE) LABORATORY PRACTICUM - 4 DO NOT CONSULT WITH OTHER LABORATORY STUDENTS, THE LABORATORY INSTRUCTOR OR GRADUATE ASSISTANT UNLESS AN ISSUE OF SAFETY, EQUIPMENT NEEDS, OR EQUIPMENT FAILURE OCCURS. You may consult your laboratory notebook or the reference books in the laboratory You may take up to 150 minutes to carry out the procedure, complete your notebook writeup on the experiment, and submit to the instructor the notebook and clearly labeled product. THE MATERIALS...

  • Construct a flow chart describing the seperation of the mixture and the isolation of each compound...

    Construct a flow chart describing the seperation of the mixture and the isolation of each compound in this experiment. (Lab steps/procedures includes for reference) 4. Construct a flow chart describing the separation of the mixture and the isolation of each compound in this experiment. A commonly used method of separating a mixture of organic compounds is known as liquid-liquid extraction. Most reactions of organic compounds require extraction at some stage of product purification. In this experiment you will use extraction...

  • Part A of experiment: Working in the fume hood, combine 4.0 mL of 10% NaOH solution and 4 mL EtOH in a 50 mL round bot...

    Part A of experiment: Working in the fume hood, combine 4.0 mL of 10% NaOH solution and 4 mL EtOH in a 50 mL round bottom flask. Dissolve 1.0 mL (8.6 mmol) of acetophenone into your solution. Add 1.0 mL (9.8 mmol) of benzaldehyde and a magnetic stir bar to your flask. Clamp the flask above a stir plate. Monitor the reaction for 45 minutes by TLC. Acetophenone needs to be diluted prior to TLC, and cannot be spotted neat....

  • 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...

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
ADVERTISEMENT