are amides more water soluble than esters and why?
Homework Answers
The electron deficiency of Carbon with double bond of Oxygen in ester is more when compared the one in Amide group.
So when dissolved in water the OH- ions in water react faster and more with ester than amide.So the solubulity of ester is more than solubulity of amide
(7 points) Explain why esters are more reactive towards nucleophilic acyl substitution compared to amides. Your...
(7 points) Explain why esters are more reactive towards nucleophilic acyl substitution compared to amides. Your answer should be clear and concise. Writing more than necessary only increases the odds of writing an incorrect statement, which could result in points off. nucleophilic acyl substitution Nu R X R Nu - - - - - - - - - - O RO R NO Ester Amide
Why is Butyric acid more water soluble than palmitic acid?
Why is Butyric acid more water soluble than palmitic acid?
Which salts will be more soluble in an acidic solution than in pure water? Explain why...
Which salts will be more soluble in an acidic solution than in pure water? Explain why each salt is or is not more soluble in an acidic solution than in pure water. CuCl CsClO4 CaSO4 Be(OH)2 AlPO4
Why do esters, carboxylic acids and amides undergo acyl substitution but aldehydes and ketones cannot?
Why do esters, carboxylic acids and amides undergo acyl substitution but aldehydes and ketones cannot?
please explain 1. Why is the conjugate base of aspirin more soluble in water than...
please explain
1. Why is the conjugate base of aspirin more soluble in water than ether? 2. Why does the extraction of aspirin by NaHCO3 generate a gas? 3. Assume 1 g of the 3 g is aspirin. Show by calculation that 7 mL of 6 M HCI is enough to completely neutralize the conjugate base of aspirin to the neutral compound.
Are patients more prone to have water soluble or fat-soluble vitamin deficiencies? Why?
Are patients more prone to have water soluble or fat-soluble vitamin deficiencies? Why?
Could you explain why too? Thank you. Which of the compounds is more soluble in an acidic solution than in pure water? C...
Could you explain why too? Thank you.
Which of the compounds is more soluble in an acidic solution than in pure water? CuBr Zn(OH)2 Srs CuCN RbC104
The reactivity sequence of carboxylic acid derivatives (acyl halides, anhydrides, acids, esters, amides) changes with t...
The reactivity sequence of carboxylic acid derivatives (acyl halides, anhydrides, acids, esters, amides) changes with the substituent. Acyl chlorides are most reactive, amides are least reactive. 1) Explain in detail why the reactivity changes in that sequence, 2) Where do carboxylates fit in that sequence and why? How does that impact on the way carboxylic acid reactions need to run? 3) Where do thioesters, RC(-O)SMe and acyl phosphates, RC(-O)OPO2OR fit in that sequence. Explain your decision
The reactivity sequence of...
3. Give a brief explanation why acid chlorides are more reactive than esters in a nucleophilic...
3. Give a brief explanation why acid chlorides are more reactive than esters in a nucleophilic substitution reaction, like a polymerization. Grading Scheme
Which of the following compounds will be more soluble in acidic solution than in pure water?!...
Which of the following compounds will be more soluble in acidic solution than in pure water?! O Cul O PbCl2 Ca(CIO), O Fes O None of the above will be more soluble in acidic solution.
(7 points) Explain why esters are more reactive towards nucleophilic acyl substitution compared to amides. Your answer should be clear and concise. Writing more than necessary only increases the odds of writing an incorrect statement, which could result in points off. nucleophilic acyl substitution Nu R X R Nu - - - - - - - - - - O RO R NO Ester Amide
please explain
1. Why is the conjugate base of aspirin more soluble in water than ether? 2. Why does the extraction of aspirin by NaHCO3 generate a gas? 3. Assume 1 g of the 3 g is aspirin. Show by calculation that 7 mL of 6 M HCI is enough to completely neutralize the conjugate base of aspirin to the neutral compound.
Are patients more prone to have water soluble or fat-soluble vitamin deficiencies? Why?
Could you explain why too? Thank you.
Which of the compounds is more soluble in an acidic solution than in pure water? CuBr Zn(OH)2 Srs CuCN RbC104
The reactivity sequence of carboxylic acid derivatives (acyl halides, anhydrides, acids, esters, amides) changes with the substituent. Acyl chlorides are most reactive, amides are least reactive. 1) Explain in detail why the reactivity changes in that sequence, 2) Where do carboxylates fit in that sequence and why? How does that impact on the way carboxylic acid reactions need to run? 3) Where do thioesters, RC(-O)SMe and acyl phosphates, RC(-O)OPO2OR fit in that sequence. Explain your decision
The reactivity sequence of...
3. Give a brief explanation why acid chlorides are more reactive than esters in a nucleophilic substitution reaction, like a polymerization. Grading Scheme
Which of the following compounds will be more soluble in acidic solution than in pure water?! O Cul O PbCl2 Ca(CIO), O Fes O None of the above will be more soluble in acidic solution.
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