Question

1.) Please explain the importance of the Ficsher Esterfication reaction. 1-3 sentences will be sufficient. 2....

1.) Please explain the importance of the Ficsher Esterfication reaction. 1-3 sentences will be sufficient.

2. Which one in more soluble in water, propanoic acid or 1,3-propanedioic acid? Please explain why? 1-2 sentences will be sufficient.

3.) Name all of the functional groups that can undergo hydrolysis, and give the corresponding products. Also, include any conditions per reaction.

0 0
Add a comment Improve this question Transcribed image text
Know the answer?
Add Answer to:
1.) Please explain the importance of the Ficsher Esterfication reaction. 1-3 sentences will be sufficient. 2....
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
  • 1.) Please explain the importance of the Ficsher Esterfication reaction. 1-3 sentences will be sufficient. 2....

    1.) Please explain the importance of the Ficsher Esterfication reaction. 1-3 sentences will be sufficient. 2. Which one in more soluble in water, propanoic acid or 1,3-propanedioic acid? Please explain why? 1-2 sentences will be sufficient. 1.) Name all of the functional groups that can undergo hydrolysis, and give the corresponding products. Also, include any conditions per reaction. 2. What do carboxylic acids and carboxylic esters have in common in regards to reduction?

  • Unsaturated hydrocarbon 1. Describe the type of reaction (ex: hydration, oxidation, hydrolysis, etc.) 2. Show a...

    Unsaturated hydrocarbon 1. Describe the type of reaction (ex: hydration, oxidation, hydrolysis, etc.) 2. Show a general equation for the reaction type and illustrate what happens in the reaction – use multiple colors, arrows, identify functional groups, etc. 3. Illustrate what happens in your specific reaction. Show both the names and the structural formulas for the reactants and the products. Use multiple colors, arrows, identify functional groups, etc. to explain how the reaction occurs. Number the parent chains and identify...

  • those I choose is wrong please help Amides are formed from the reaction of carboxylic acids...

    those I choose is wrong please help Amides are formed from the reaction of carboxylic acids with 1° amines carboxylic acids with 2 amines carboxylic acids with 3 amines Only A and B All of the above What are the hydrolysis products of N-methylpropanamide? propanoic acid and methylamine propanoic acid, methylamine, and water propanoic acid and ammonia

  • What is the importance of the 2′ hydroxyl group in the ribose sugar of an RNA...

    What is the importance of the 2′ hydroxyl group in the ribose sugar of an RNA molecule? Check all that apply. View Available Hint(s) Hint 1. Properties of an hydroxyl groupopened hint A hydroxyl group has the formula OH. Water, alcohols, carboxylic acids, and other hydroxy-containing compounds can be deprotonated owing to the high electronegativity of oxygen, resulting in a stable conjugate base. Hydroxy-containing compounds are also able to form hydrogen bonds, which lead to higher boiling and melting points...

  • (2) Diels-Alder reactions of a diene with a dienophile are known to undergo a concerted reaction....

    (2) Diels-Alder reactions of a diene with a dienophile are known to undergo a concerted reaction. However, 2,3-Di- tert-1,3-butadene does not undergo Diels-Aider reactions. Explain 2,3-di-tert-1,3-butadiene (4) Propose mechanisms for the following steps 1 and 2. Slep 1 Step 2 Bry Br NaBH CH acetic acid (I) Using> as a symbol, rank the following alkyl bromides in order of decreasing reactivity. (6 pts) Br Cн,Br -Br (a) For hydrolysis by an Sy1 mechanism (b) For hydrolysis by an S,2 mechanism...

  • Can someone help with the 4 POST LAB questions thanks Carboxylic Acids and Esters acid). like...

    Can someone help with the 4 POST LAB questions thanks Carboxylic Acids and Esters acid). like citric acid. Face crearboxyl the name implies, a Carbexylic Aclds A salad dressing made of The sour taste of fruits such as lemons is due to the presence of acids like citric acid. tcarboxyl a-hydroxy acids such functional group - that is, a carbonyl group attached to a hydroxyl group. AS dicarboxylic acid carboxylic acid of benzene is called benzoic acid (Figure 1). oil...

  • answer all please Find information on: 1. ascorbic acid 2. codeine 3. cinnamaldehyde 4. pethidine To...

    answer all please Find information on: 1. ascorbic acid 2. codeine 3. cinnamaldehyde 4. pethidine To get full credit (4 pts) you must: 1. Give molecular formula, structure, and identify of all functional groups. 2. Identify configurations (if present) within the molecule, e.g. (R/S, E/Z, cis/trans). 3. Propose a reaction (1 rxn) that could transform the molecule (or part of the molecule, i.e. functional group) into a new compound (show the new compound). 4. Identify the molecule's importance and/or application

  • When an aldehyde or ketone undergo a nucleophilic attack, the reaction follows a nucleophilic addition mechanism....

    When an aldehyde or ketone undergo a nucleophilic attack, the reaction follows a nucleophilic addition mechanism. Conversely, carboxylic acids and their derivatives are known to undergo nucleophilic acyl substitution. Even though all of these functional groups are defined by the carbonyl group, they react very differently. In 1-3 sentences, explain why an aldehyde and a carboxylic acid derivative follow different mechanistic pathways in the presence of a nucleophilic species.

  • write the con Chapter 16 Carboxylic Acids and Esters Name: 1) Write the condense structural formulas...

    write the con Chapter 16 Carboxylic Acids and Esters Name: 1) Write the condense structural formulas of the following compounds: Date: 3 methylpentanoic acid p-ethylbenzoic acid 4 m-hydroxylhexanoic acid 2) Which of the following compounds has the higher boiling point: butane, butanol, butanoic acid, and methyl ethanoate? Briefly explain why. 3) From the compounds of previous question, which is more soluble in water? Briefly explain why 4) Give the name of the carboxylic acid and alcohol used to prepare the...

  • CHE 201 1. Give two reasons why concentrated sulfuric acid was added to the reaction 2....

    CHE 201 1. Give two reasons why concentrated sulfuric acid was added to the reaction 2. In the synthesis of homohutano why was Synthesis of bromobutane why was the reaction mixture cooled in an ice bath before a concentrated sulfuric acid2 Describe what might happen if you forgot to cool the mixture. the esterification of butanol hu ur side products in the synthesis of hom feng butul hydrogen sulfate (A). This causes decreasing the yield of the desired product e...

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