Question

This question has multiple parts. Work all the parts to get the most points. For the following reaction: с 1. NaOCH CH3 Hoc о
b Write a mechanism for the step shown below, using curved arrows to show electron redistribution. Arrow-pushing Instructions
X CH CH. CH2CH, HH Draw the product of the mechanism step in part (b) above. • Do not include counter-ions, e.g., Na, r, in y i answered part A and B . i need the answer to part C. please clearly identify the answer and write out everything
0 0
Add a comment Improve this question Transcribed image text
Answer #1

Answer: for Part B. Part to c you should Stent with & Toch cuz y con ferung occuz. T - CH₂ CH2-04 - segons on o cu, cuz o cucthe structure of both (c) is a resonating structure so all the structure are correct.  

i hope you understand the solution

please rate this answer :)

Add a comment
Know the answer?
Add Answer to:
i answered part A and B . i need the answer to part C. please clearly...
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
  • b) write rhe mexhanism for the step below This question has multiple parts. Work all the...

    b) write rhe mexhanism for the step below This question has multiple parts. Work all the parts to get the most points. For the reaction below: NH, OCH CH3 pyridine a Draw a structure for the organic products). • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right comer CP OOO OO O OO. * Correct i n CH3CH2OH CHOIS b Write a mechanism for the step below, using curved arrows to show...

  • 0 () CH,CH CCH,-C-OCH, NocCH (2) CH (3) Ho .heat (I) NaOCH2CH (2) H,O', heat (b) CH,-C-CH-C-OCH,C...

    predict the products of the following reactions 0 () CH,CH CCH,-C-OCH, NocCH (2) CH (3) Ho .heat (I) NaOCH2CH (2) H,O', heat (b) CH,-C-CH-C-OCH,CH,+ CH, (1) LDA -OH (c) Ph CH, () CH,CH,CH,Br (1) H2C-CH CH,Br (2) H0* OCH, NaOCH Ph (2) CH,CH,CH2CH2Br (g) product from part (f) (decarboxylation) 0 () CH,CH CCH,-C-OCH, NocCH (2) CH (3) Ho .heat (I) NaOCH2CH (2) H,O', heat (b) CH,-C-CH-C-OCH,CH,+ CH, (1) LDA -OH (c) Ph CH, () CH,CH,CH,Br (1) H2C-CH CH,Br (2) H0*...

  • Be sure to answer all parts. Draw the products in the following reaction. CH,CH,OH C4,C4,04 Part 1: Identify which...

    Be sure to answer all parts. Draw the products in the following reaction. CH,CH,OH C4,C4,04 Part 1: Identify which mechanism(s) the reaction will undergo. Syl S2 E1 E2 Part 2: The number of Syl product(s): 1 The number of El product(s): 2 Part 3 out of 3 CH2CH3 The Syl product: edit structure ... The El products: edit structure ... draw structure ... (product with methyl group) (product with ethyl group)

  • The answers C and E are incorrect for above. The question is asking for the *precursor*...

    The answers C and E are incorrect for above. The question is asking for the *precursor* of ethylamine, please state which option is correct. Also include full synthesis and reagents. I need help for part 3. I put just H3O+ and it was incorrect. Please write the correct answer/answers! I will give thumbs up if you complete both with right answers! Choose the best option for the precursor to ethylamine. CH3CH2 CH2CH NH2 N OCH2CH3 OCH2CH3 A (CH,CH),NH C CHUCH...

  • Please help me!!! 17. (15) Draw the reaction occur Draw the major product or products of each of the following react...

    Please help me!!! 17. (15) Draw the reaction occur Draw the major product or products of each of the following reactions indicate whether Ction occurs by an Syl,S2, E. or E, mechanism on the line provided. Be sure to include stereochemistry in your answers where it is appropriate OH a. mech: H2SO4 b. mech: - KOC(CH) HOC(CH3) c. mech: CH,CH,OH 40° KCN H20 d. mech: OH BI c. mech I Hot Cho con un Nal acetone (aq) 40 °C HC-CH2CH3...

  • I only need part B 4C ids as well as other small Juable starting materials in Id effect the following trans 3.5. Substa...

    I only need part B 4C ids as well as other small Juable starting materials in Id effect the following trans 3.5. Substances such as carbohydrates and amino acids. molecules available from natural sources are valuable enantiospecific syntheses. Suggest reagents that could effe formations, taking particular care to ensure that the produ ically pure. he product will be enantion нон O ll CN(CH3)2 from OH CHO (CH3)2NC носна CO₂CH₂ CH30, OH (b) CHOOCH ) H OCH HOCH СН,ОН from HOCHZ...

  • i need help with b,e, and f please! 2) Fill in each of the following boxes...

    i need help with b,e, and f please! 2) Fill in each of the following boxes with the structure of the major reaction product(s) from each of the following reactions. If you believe that no reaction will take place, write NR in the box (28 points total) BO PSPP) NaOH Pd OA) (CH.CH N.R. bi OCH Brin Ho CO2H H OH HFoH MOCOH нон CH OH CH₂OH H OH CO2H НО 애 Coat сно на H OH HO+H H- OH...

  • Part A has been solved. The issue is Part B. This question has multiple parts. Work...

    Part A has been solved. The issue is Part B. This question has multiple parts. Work all the parts to get the most points. For the reaction below: НСІ H20 a Draw the product(s). • Include counter-ions, e.g. Na 1. in your submission, but draw them in their own separate sketcher. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. I . Học H, cũ + H3c—ÑHz Cí b Use curved...

  • please help, i dont know what im doing wrong. thank you! Be sure to answer all...

    please help, i dont know what im doing wrong. thank you! Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: Brz (1 equiv) Part 1 out of 2 nces OOO edit structure. edit structure - Check my work Next part 1 attempt left

  • I need some help with part b in the question please (a) Propose a one-step mechanism...

    I need some help with part b in the question please (a) Propose a one-step mechanism using curved arrow notation for the formation of styrene oxide from styrene using MCPBA, as shown below. (b) Propose a step-wise mechanism using curved arrow notation for reaction of styrene oxide with (CH_3)_2 CHNH_2 that includes the structure of the expected product. To simplify the mechanism, do not show formation of enantiomers.

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