ZuoTi.Pro
Question
Can you explain this in very much detail including background theory and things I have to know to solve this?
The reaction below would go via: он о CN DMF PRODUCT(S) A. SN1 mechanism with inversion B. SN1 mechansim with racemic product
science   chemistry   
0 0
Add a comment Improve this question Transcribed image text
Next > < Previous
Sort answers by oldest

Homework Answers

Answer #1

Answer:

- Su NG H 8) NCO CH3 Cyanide ion attacks from rear side and a good leaving group departs. The Sn2 mechanism ivolved here as i

==================XXXXXXXXXXX===================

0 0
Add a comment
Know the answer?
Add Answer to:
Can you explain this in very much detail including background theory and things I have to...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Log In

Sign Up

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

  • Can you explain this in very much detail including background theory and things I have to...

    Can you explain this in very much detail including background theory and things I have to know to solve this? What is the product? CH30 CH3OH A. OCH, BHOLE-OCH. Mo OH | A.A B.B C.C D.D E. E HC HEC HC D. Hgco H2 НЕС-он E none of the above нс IS

  • Can you explain this in very much detail including background theory and things I have to...

    Can you explain this in very much detail including background theory and things I have to know to solve this? Which of the following cannot undergo nucleophilic substitution reactions? A. CH2 CHCH,Br с. CH2 Br Br Br Е. Br D. В.

  • Can you explain this in very much detail including background theory and things I have to...

    Can you explain this in very much detail including background theory and things I have to know to solve this? What is the product? H2SO4 CH3 H нус-с-с-сң CH, OH А. сн. н в. в не сн с. нс. н. с-с-сн, р. A and в E. B and C нэс-с-с-с-н нс сн ныс сн. сн,

  • will you please check the ones i did also. 12. (I pt each) Each of the...

    will you please check the ones i did also. 12. (I pt each) Each of the following reactions gives a substitution product. lIdentify the major product in each case and indicate whether the reaction is likely to proceed via a bimolecular (Su2) or a unimolecular (S1) mechanism. S1 OF 9,2 Br NaCN DMF SNI EtOH Aprotc Sy1 or SN2? он CH3 CHs он SN1 or SN2? electrophile nucleophile Br ONa DMF SN1 or Sy2? prot℃

  • Could someone please explain how to do this. Thank you. If you could explain in detail...

    Could someone please explain how to do this. Thank you. If you could explain in detail so I could understand I would appreciate it very much! Provide curved arrows to indicate the mechanism involved in each step of the following Hantzsch pyridine synthesis. 0 OH OH OH 0 он о O HO NH3 OH O H2N он он OH H

  • can you please explain these 2 questions with detailed explanation and background theory both? 2 6:35...

    can you please explain these 2 questions with detailed explanation and background theory both? 2 6:35 11 5 R 51%1 chapter_12_powerpoint_I. ppt What is the product of reaction below? 1) CH COH 2) -Он/н-0 но, Е. но. но В. A. но но но Determine the product. mCPBA Н н OH он он Нас. CHs C Н,с- CH3 Нас-сн D. A. H3C CH B н н Н Н E. none of the above

  • can someone please explain how to do this with as much detail as possible. someone tried...

    can someone please explain how to do this with as much detail as possible. someone tried to explain it earlier in relation to (a,e) and (e,a) but im not sure even what that means Bccurance of Methyl shift o. The following two elimination reactions are found to have very different rates of reaction. The cis compound produces two products and it reacts much faster than the trans isomer, which produces only one product. Explain these observations (the erence in rate...

  • Please explain each choice in detail. Thank you very much. 1. What can we say about...

    Please explain each choice in detail. Thank you very much. 1. What can we say about a time series given its sample autocorrelation function? An actuary produces the following sample ACF for vehicle accident severities over a 10-year period: 10 06 ACF 02 -52 0 5 10 15 20 25 30 30 You are also given the following three statements about this time series: I. There is a positive trend in accident severity; II. There is a negative trend in...

  • how do i know which Hydrogens i affect? what do i do here? can someone explain...

    how do i know which Hydrogens i affect? what do i do here? can someone explain what im supposed to be looking for with drawings too? i thought this was an aldol condensation but this says its a michael reaction and the answer is C. thank you so much! 290. Predict the product: CH2=CH-C + OH CH=CH-C°. CH-&-CH2-8-CzHs Hot H2O H O=0 -C-C-C2H5 о но No reaction: base is too weak to allow deprontonation. CH2 e) C2H5-C-C-C-C2H5 CH2 HG он...

  • Could you please explain how do I do these type of questions in general? I have...

    Could you please explain how do I do these type of questions in general? I have no idea what goes in or out of the reaction and why. Would be nice if you could go in detail to even the most basic things, thank you! B2. Consider the reactions shown below: 1. EtMgBr (excess) diethyl ether Me 2. H20, HCI Ph Et O reagent(s) 10 Me Et " Product 2 Product 1 a) Draw the structure of organic Product 1...

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