Question

a sample of crude organic product isolated from a reaction is insoluble in boiling toluene (methylbenzene)....

a sample of crude organic product isolated from a reaction is insoluble in boiling toluene (methylbenzene). explain whether toluene would be an appropriate solvent for the recrystallization of the crude product.

Homework Answers

Answer #1

The basic theory of the recrystallization process is following :

To remove insoluble impurities; dissolved in a solvent, the solution is filtered to remove the insoluble impurities, and the solvent evaporated to produce the solid compound.

To remove colored impurities do same process with an additional step. The solid is dissolved in a solvent and activated charcoal is added, the solution is filtered as before, and the solvent is evaporated to produce the solid compound.

To remove these impurities by the recrystallization process solvent has

high solubility at high temperatures and low solubility at low temperatures.

Here sample of crude organic product isolated from a reaction which is insoluble in boiling toluene (methylbenzene) means sample is insoluble in toluene. If the solid is not dissolved in this than recrystallization of the solid not possible.

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
2. You have carried out a synthesis reaction and isolated the solid crude product. Scrutiny of...
2. You have carried out a synthesis reaction and isolated the solid crude product. Scrutiny of its 1H NMR spectrum indicates the presence of an impurity, which you estimate to be approximately 6-8% of the total sample. You decide to purify it via recrystallization and know that you will first need to determine which solvent or solvent pair would be suitable. Describe what you would do and how you would evaluate your results. What properties of the solvent would you...
Can someone please look over my short paragraph about my organic laboratory experiment for any edits...
Can someone please look over my short paragraph about my organic laboratory experiment for any edits on making it more detailed yet concise at the same time. For example, I'm not sure if I should include that acetonitrile and toluene should be stated that they were insoluble compared to the other three solvents just for claification? The purpose of this second laboratory experiment was to determine a proper solvent for recrystallization of acetaminophen by using the solubility properties in five...
Recrystallization Step: The procedure asks for using equal amount by mass of the crude product and...
Recrystallization Step: The procedure asks for using equal amount by mass of the crude product and the recrystallization solvent, 95% ethanol. Suppose you use 1.2g of product, how many mL of 95% ethanol would you add? Write the answer with 3 significant figures (e.g. 2.15). Density of 95% ethanol = 0.86 g/mL
In an experiment where students are isolating Acetylsaliclic Acid (ASA) from Aspirin tablets, would recrystallization work...
In an experiment where students are isolating Acetylsaliclic Acid (ASA) from Aspirin tablets, would recrystallization work if you had 5 grams of an impurity contaminating 1 gram of your desired product and both were soluble in the recrystallization solvent at its boiling point and insoluble at room temperature? Why or why not?
During work up of the SN1 reaction, the organic product separates from the aqueous layer upon...
During work up of the SN1 reaction, the organic product separates from the aqueous layer upon standing in a separatory funnel. State whether the organic product forms the upper or lower layer and briefly explain your choice. The SN1 treatment involves treatment of 2-methyl-2 butanol with HCL to synthesize 2-chloro-2-methylbutane
After re-weighing your crude 4-bromoacetanilide (214.06 g/mol), you obtain 163 mg of crude product. After recrystallization,...
After re-weighing your crude 4-bromoacetanilide (214.06 g/mol), you obtain 163 mg of crude product. After recrystallization, you isolate 121 mg of pure product. If you started with 125 mg of acetanilide (135.17 g/mol), calculate the percent yield of 4-bromoacetanilide (214.06 g/mol) for this reaction. Assume an excess of bromine. Enter your answer as digits only, no percent sign, using the proper number of significant figures. Can you please explain it step by step. Reaction: Acetanilide + Br2 >>>>>>>CH3COOH with room...
LLE is often performed to separate an organic product from a reaction mixture. Diethyl ether is...
LLE is often performed to separate an organic product from a reaction mixture. Diethyl ether is used in this oxidation reaction. Why is more thanone extraction of the aqueous layer required? Explain on a microscopic level.
A sample of 4-toluic acid is contaminated with a small amount of sand & toluene. Using...
A sample of 4-toluic acid is contaminated with a small amount of sand & toluene. Using active extraction (changing the polarity by addition of certain chemicals) & a gravity filtration to remove a component, describe how you would obtain pure 4-toluic acid in its solid form from this mixture. Note that use of an organic solvent like ether should be used initially, & then any other procedures, including use of a separatory funnel is required.
how do i find yield of crude product obtained in the reaction? and how do i...
how do i find yield of crude product obtained in the reaction? and how do i find theoretical yield in grams and percent yield. let's say my grams after recrystallization is .769 grams . I converted acetanilide to p-bromoacetanilide. I have a recyrstallized p-bromoacteanilide after finsihing the experiement. I want to know this infomration for my 0.769 grams of p-bromoactenalidie that i have after finsihging the xperiment.
What product would result from the reaction of (R)-2-bromooctane with – CN, in a DMSO solvent?...
What product would result from the reaction of (R)-2-bromooctane with – CN, in a DMSO solvent? What is the stereochemistry of the product? Explain your answer to the stereochemistry question by writing a detailed mechanism for this reaction. Why is DMSO a good solvent for this reaction? (2 points)