If you mix a neutral compound dissolved in an organic solvent with aqueous base describe what...
If you mix a neutral compound dissolved in an organic solvent with aqueous base describe what will happen.
a. Will a proton get transferred during this process?
b. In which solvent, the organic or aqueous solvent, will the neutral compound more likely be after mixing?
Homework Answers
a) There will be no proton transfer in this process as the neutral compound does not react with acid or base
b) The neutral compound will most likely to be in organic solvent.
Add Answer to:
If you mix a neutral compound dissolved in an organic solvent
with aqueous base describe what...
If you have an aqueous solution containing an organic acid salt and a neutral compound, which...
If you have an aqueous solution containing an organic acid salt and a neutral compound, which one will be extracted into ethyl acetate upon mixing in a separatory funnel?
Acidic compound: Ethyl 4 aminobenzoate Neutral compound: Fluorenone (12 points). Separation Scheme:_(5 points for the aqueous...
Acidic compound: Ethyl 4 aminobenzoate
Neutral compound: Fluorenone
(12 points). Separation Scheme:_(5 points for the aqueous extract or layer and 7 points for the organic extract or layer). By drawing the actual structures of the neutral compound that you have identified and either the acidic or basic compound or impurity present in your mixture, write a separation scheme for this binary mixture. Draw the appropriate complete structures with the correnct number of unshared electrons and/ or charges if any during...
Extraction Q1. Why doesn’t the neutral organic compound dissolve in the 1.5 M NaOH solution? Q2....
Extraction Q1. Why doesn’t the neutral organic compound dissolve in the 1.5 M NaOH solution? Q2. Why is diethyl ether a good choice for the organic solvent in this extraction experiment? Q3. What experimental difficulty would you encounter if you neglected to include the drying step before evaporating the ether solution of the neutral organic compound? Q4. Why are the two organic compounds recrystallized before their melting points are determined? Q5. What IR bands are most useful in distinguishing a...
Explain the acid/base chemistry that occurred when you separated the organic base and neutral compound. Include...
Explain the acid/base chemistry that occurred when you separated the organic base and neutral compound. Include chemical equations. The two compounds used were 1,4-dichlorobenzene and ethyl 4-aminobenzoate.
Explain the acid/base chemistry that occurred when you separated the organic base and neutral compound. Include...
Explain the acid/base chemistry that occurred when you separated the organic base and neutral compound. Include chemical equations. The two compounds used were 1,4-dichlorobenzene and ethyl 4-aminobenzoate.
Answer the following before coming to lab: 1.) Based on what you saw last week, which...
Answer the following before coming to lab: 1.) Based on what you saw last week, which enantiomer of tartaric acid would you expect to co- crystallize with (SS)-1,2-diammoniumcyclohexane? 2.) If you had a neutral aqueous solution of triethylamine, would you add acid or base in order to extract it with an organic solvent? 3.) Now, consider a dichloromethane solution of triethylamine. Would you extract with acidic aqueous or basic aqueous solution in order to get the triethylamine out of the...
A three-component mixture of organic compounds in diethyl ether consists of a carboxylic acid, an amine...
A three-component mixture of organic compounds in diethyl ether consists of a carboxylic acid, an amine base, and a neutral compound. After treatment with 3 M HCl and thorough mixing, what compound(s) will be present as major components of the aqueous phase? a)the neutral compound b)the carboxylic acid and the neutral compound c)the amine d)the amine hydrochloride salt
Complete the rxn equations that place with your analyte compound when you extracted with aqueous base...
Complete the rxn equations that place with your analyte compound
when you extracted with aqueous base solution. Write NR if analyte
compound doesnt react. Indicate which layer, organic or aqueous
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Name: Date: Separation of Acid/Base/Neutral compounds using liquid-liquid extraction OCH CHO HN Benzocaine Molecular Weight: 165.19...
Name: Date: Separation of Acid/Base/Neutral compounds using liquid-liquid extraction OCH CHO HN Benzocaine Molecular Weight: 165.19 Melting Point: 88-90 °C 1,1-biphenyl Molecular Weight: 154.21 Melting Point: 68-70 °C trans-cinnamic acid Molecular Weight: 148.16 Melting Point: 132-135 °C Question 1: Identify the following compounds as Acid, Base or Neutral. (2 points) a. Benzocaine: b. Biphenyl: c. Trans-cinnamic acid: (2 points) _ (2 points) Question 2: Draw the structure in the box (5 points each): NaOH OCH,CH, HCM NaOHA HC form. Ples...
1)When you perform a liquid-liquid extraction using a separatory funnel, which of the following organic solvent...
1)When you perform a liquid-liquid extraction using a separatory funnel, which of the following organic solvent is on the bottom of the aqueous phase and which is on top? (write your answer by the solvent name) a) Ethyl acetate b) hexane c) Dichloromethane d) diethyl ether 2) If you are performing a liquid-liquid extraction and you have a mix of a carboxylic acid and a non-acidic compound, which combination of solvents would you use for the separation? a) dichloromethane/HCI b)...
Acidic compound: Ethyl 4 aminobenzoate
Neutral compound: Fluorenone
(12 points). Separation Scheme:_(5 points for the aqueous extract or layer and 7 points for the organic extract or layer). By drawing the actual structures of the neutral compound that you have identified and either the acidic or basic compound or impurity present in your mixture, write a separation scheme for this binary mixture. Draw the appropriate complete structures with the correnct number of unshared electrons and/ or charges if any during...
Answer the following before coming to lab: 1.) Based on what you saw last week, which enantiomer of tartaric acid would you expect to co- crystallize with (SS)-1,2-diammoniumcyclohexane? 2.) If you had a neutral aqueous solution of triethylamine, would you add acid or base in order to extract it with an organic solvent? 3.) Now, consider a dichloromethane solution of triethylamine. Would you extract with acidic aqueous or basic aqueous solution in order to get the triethylamine out of the...
Complete the rxn equations that place with your analyte compound
when you extracted with aqueous base solution. Write NR if analyte
compound doesnt react. Indicate which layer, organic or aqueous
each would be
compound does not react. Indicate which layer, organic or aqueous, eac base extraction. Hoy NO₂ con O-H OO-H HN "NO2
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1)When you perform a liquid-liquid extraction using a separatory funnel, which of the following organic solvent is on the bottom of the aqueous phase and which is on top? (write your answer by the solvent name) a) Ethyl acetate b) hexane c) Dichloromethane d) diethyl ether 2) If you are performing a liquid-liquid extraction and you have a mix of a carboxylic acid and a non-acidic compound, which combination of solvents would you use for the separation? a) dichloromethane/HCI b)...
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