Question

1. Why does sodium benzoate dissolve so well in water, whereas benzoic acid does not? 2....

1. Why does sodium benzoate dissolve so well in water, whereas benzoic acid does not?

2. Explain how the two compounds (benzyl alcohol and benzoic acid) partition between ether and a NaOH solution in the manner that they do. HINT: Why are they soluble in the layers that they are in, and not the other?

Homework Answers

Answer #1

1. sodiumbenzoate is a salt. It is pure ionic compound. So it ionizes very well in water and solubilise easily. Where as benzoic acid is organic acid compound, it will not soubilise compleatly in water.

2.benzoic acid will partition into aqueous NaOH solution and benzyl alcohol into the ether layer.

Because, benzoic acid make salt as sodium benzoate with NaOH solution. Benzoic acid is an acid and it reacts with NaOH base to form salt. It will soluble in water

Benyl alcohol is organic compound. It is non polaric in nature. It will soluble in non polar solvent like ether.

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
Why is sodium benzoate easily extracted into H2O, while benzoic acid is not extracted into H2O?...
Why is sodium benzoate easily extracted into H2O, while benzoic acid is not extracted into H2O? How do you know which ionic compounds are soluble in water?
Why does benzoic acid not dissolve in water or HCl acid, but completely dissolves in NaOH?
Why does benzoic acid not dissolve in water or HCl acid, but completely dissolves in NaOH?
You are given a vial containing a mixture of the following compounds 1-naphthol Benzoic acid Butyl...
You are given a vial containing a mixture of the following compounds 1-naphthol Benzoic acid Butyl acetate Indole Assume the compounds are soluble in (diethyl)ether and have limited (slight) water solubility. Plan the separation of the compounds by extraction. You have a separatory funnel, your lab drawer, shared equipment, and the following reagents to use Ether 5% NaOH 10% NaHCO3 5% HCl 12M HCl 6M NaOH Na2SO4(s) 1.Describe the plan in words. Outline or describe the extraction(s) needed to separate...
Why does the sequence for extracting the diethyl ether solution of benzoic acid, naphthalene, and 1-naphthol...
Why does the sequence for extracting the diethyl ether solution of benzoic acid, naphthalene, and 1-naphthol start with aqueous bicarbonate and follow with aqueous hydroxide rather than the reverse order?
1. If one wanted to reduce the solubility of benzoic acid in water to get it...
1. If one wanted to reduce the solubility of benzoic acid in water to get it better partitioned into diethyl ether, would it be better to add potassium carbonate or sodium chloride? WHY? Please explain in terms of anions! 2. Even if a cospotted TLC analysis of an unknown with an authentic standard is performed, one still does not know with complete certainity that the unknown and the standard are identical. Why is this true? What alternatives would one consider...
Why are the standard molar enthalpies for benzoic acid and biphenyl so different? Explain this in...
Why are the standard molar enthalpies for benzoic acid and biphenyl so different? Explain this in terms of bonds formed and broken in the individual combustion reactions. Identify two specific functional groups (think organic chemistry) that contribute to the enthalpic differences between these two compounds.
1a) Why can Methanol not be used as a solvent with water as the other solvent...
1a) Why can Methanol not be used as a solvent with water as the other solvent in extraction. 1b) explain why multiple extractions with smaller volumes of the extractionsolvent are typically better than single extractions with larger volume of the solvent. 1c) Benzoic acid is a much stronger acid than the weak acid phenol (C6H5OH) consequently benzoic acid reacts with the weak base sodium bicarbonate, NaHCO3, while phenol does not. Suggest a scheme for the total separation of the three...
Procedure Experiment 1: Standardize an NaOH Solution Using Benzoic Acid as Primary Standard Part 1: Prepare...
Procedure Experiment 1: Standardize an NaOH Solution Using Benzoic Acid as Primary Standard Part 1: Prepare the NaOH Solution Take a 250 mL volumetric flask from the Containers shelf and a balance from the Instruments shelf and place them on the workbench. Zero the mass of the volumetric flask on the balance. Take sodium hydroxide from the Materials shelf and add 1 g to the flask. Record the mass from the balance display. Place the volumetric flask on the workbench....
Sodium Borohydride Reduction Reaction 1. Dissolve 600 mg of your carbonyl compound in 3 mL of...
Sodium Borohydride Reduction Reaction 1. Dissolve 600 mg of your carbonyl compound in 3 mL of methanol. Cover the flask with aluminum foil when not adding reagents or taking TLC samples to keep any water from getting in. 2. Cool your flask to 0° C using ice/water. 3. Allow to stir in the ice for 2 minutes then slowly add 0.4g of NaBH4 to your solution, then remove from ice bath and stir at room temperature. 4. After 10 min,...
Problem set for Competitive Nucleophiles 1) Why does water always enter the bottom of the condenser...
Problem set for Competitive Nucleophiles 1) Why does water always enter the bottom of the condenser and exit from the top? 2) Why are boiling stones added to the solvent undergoing reflux? 3) Why are any large clumps of ammonium salts broken down into a powder? 4) Why is it necessary to perform the competing nucleophiles reactions under acidic conditions? 5) Which is the better nucleophile, fluoride or iodide ion? Explain this in the terms of the nature of the...
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT