Question

Question 1 1 pt Which of the following is/are accurate statements concerning the mechanism shown below? Assume that liquid am

Question 1 1 pt Which of the following is/are accurate statements concerning the mechanism shown below? Assume that liquid ammonia and enough HCI to make sufficient NH4 ion are present in the reaction mixture. Select all that apply. n The collapse of the tetrahedral intermediate represented by step 3 is incorrect because under the acid-catalyzed conditions, hydroxide ion will not be a viable leaving group. Leaving aside the issue of whether hydroxide ion would be present or not, the electron flow depicted in step 4 for the final proton transfer is not depicted properly fi.e., t does not correctly convey how hydroxide would act as a base). special characteristics (such as an empty p orbital) that would otherwise allow it to occur ammonia. - The intra-intermediate proton transfer depicted in step 2 is incorrect because it represents a 4 center, 4 electron process that does not have any a The nucleophilic attack indicated for step 1 is incorrect because the carbonyl oxygen should be protonated prior to attack on the carbonyl carbon by 1 pts Question 2 Which of the following provides an accurate statement concerning the mechanism shown below? : O
0 0
Add a comment Improve this question Transcribed image text
Answer #1

No- a он 0 0 C0SkuI step 2 our ap 3 ouf он Stor-u Intermadiate repre^erted ocut Cossecli

Add a comment
Know the answer?
Add Answer to:
Question 1 1 pt Which of the following is/are accurate statements concerning the mechanism shown ...
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
  • СО cat. H + NH2CH3 + H2CO2C CO2CH3 CO CHE Cocaine has been prepared by a...

    СО cat. H + NH2CH3 + H2CO2C CO2CH3 CO CHE Cocaine has been prepared by a sequence beginning with a Mannich reaction between dimethyl acetonedicarboxylate, methylamine, and butanedial. The mechanism involves the following steps: 1. Following initial protonation of the carbonyl oxygen, nucleophilic attack by the amine forms carbinolamine 1; 2. Proton transfer and elimination of water forms iminium ion 2; he enol form of the dicarboxylate ester attacks the iminium ion to form adduct 3; 4. Adduct 3 tautomerizes...

  • Alkyl halides may undergo elimination reactions with BrØnstead-Lowry bases in which the halide and an adjacent...

    Alkyl halides may undergo elimination reactions with BrØnstead-Lowry bases in which the halide and an adjacent proton are lost to form a new π bond. Because of the loss of a proton and a halide anion the reactions are termed ‘dehydrohalogenation’. The two most common associated mechanisms are designated as either unimolecular (E1) or bimolecular (E2) elimination reactions based on reaction rate studies. E1 reactions proceed via a two-step mechanism that involves the cleavage of the leaving group (here the...

  • Alkyl halides may undergo elimination reactions with BrØnstead-Lowry bases in which the halide and an adjacent...

    Alkyl halides may undergo elimination reactions with BrØnstead-Lowry bases in which the halide and an adjacent proton are lost to form a new π bond. Because of the loss of a proton and a halide anion the reactions are termed ‘dehydrohalogenation’. The two most common associated mechanisms are designated as either unimolecular (E1) or bimolecular (E2) elimination reactions based on reaction rate studies. E1 reactions proceed via a two-step mechanism that involves the cleavage of the leaving group (here the...

  • Under typical conditions, many essential biochemical reactions proceed so slowly that life could not exist without...

    Under typical conditions, many essential biochemical reactions proceed so slowly that life could not exist without the presence of enzymes. Enzymes increase reaction rates through a wide variety of mechanisms. These mechanisms generally utilize the following strategies: improving the nucleophiles and electrophiles present in the catalytic R groups or substrates; stabilizing the extra electron density of the leaving group; and stabilizing transition states. Proteases are enzymes that break down proteins by hydrolyzing peptide bonds. Chymotrypsin is a protease found in...

  • 1-24 need help really lost Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for...

    1-24 need help really lost Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for the following deprotonation step. Also add the other product notice how the Tema s can be converted to this by use of a strong base such as sodium a sodium ion (Na) is not drawn, in this case it is just a spectatorio PCW27 - Mechanistic steps - Part Name: Time spent 2) Label the above compounds with the appropriate name from the previous...

  • use the notes provided to help answer the question above. will rate well The second step...

    use the notes provided to help answer the question above. will rate well The second step of the synthesis transformation of the chlorosulfonyl functional group into a sulfonamide) is an example of a a. Nucleophilic displacement (substitution) b Elimination C. Electrophilic aromatic substitution d. Acid hydrolysis Esterification e. THE SULFONIC ACID GROUP AND ITS DERIVATIVES Sulfonic acids are organic analogs of sulfuric acid, a very strong acid. They are highly corrosive, react vigorously with water, and can cause skin bums....

  • please snswer all thanks 5. For the following reaction step, indicate which pattern of arrow pushing...

    please snswer all thanks 5. For the following reaction step, indicate which pattern of arrow pushing it represents. Circle one. A. proton transfer C. nucleophilic attack B. loss of leaving group D. rearrangement 6. The following reaction has three mechanistic steps (down, across, and up), Draw all of the curved arrows necessary to complete the mechanism. (Hint: there should be 4 arrows total) HBO OH Br H-Br OH2 + Hö 7. Draw the most likely structure of the following cation...

  • Questions and Exercises 1. In the course of reflux of the triglyceride in a sodium hydroxide solu...

    Organic Chemistry Help! Questions and Exercises 1. In the course of reflux of the triglyceride in a sodium hydroxide solution you will notice a lot of foaming. Explain. What is left behind in the aqueous layer after filtration of the saponification product? The starting material and the product of the saponification reaction have similar melting points. How do you know you actually isolated a new product rather than just recovered the starting material? Give at least two different methods to...

  • 1. Which of the following are the sites within the human body where carbon dioxide and...

    1. Which of the following are the sites within the human body where carbon dioxide and oxygen are exchanged? A. Alveoli B. Arteries C. Synapses D. Venules 2. Which of the following describes the most important reason for repeating an experimental investigation? A. To verify the validity of the original findings B. To expand upon the original investigation C. To manipulate the independent variable D. To attempt to disprove the hypothesis 3. Lithium has an atomic number of 3 and...

  • Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepa...

    i need help with the postlab questions please Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....

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