Question

9. Write out the mechanism for CA3 CH3OH SN 10. a) Write out 6 completely different reactions of cyclohexanone (reagent produ

Please answer the ENTIRE page. #9-11.
0 0
Add a comment Improve this question Transcribed image text
Answer #1

Write Out the mechanism en for Сн, -он SN Mec Manism involves thuo Stepts tep C-X bondd & tormaton & Rote determing step eleadiflerent 3) Write Out 3 Pre peraton 2-utanol Starting material or each me- 9ngovme prepa You jurt have Other Prep You iney h

Add a comment
Know the answer?
Add Answer to:
Please answer the ENTIRE page. #9-11. 9. Write out the mechanism for CA3 CH3OH SN 10....
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
  • question 9, 10c and 11 need answers 9. Write out the mechanism for: MSH CH₂ SNZ...

    question 9, 10c and 11 need answers 9. Write out the mechanism for: MSH CH₂ SNZ 10.) Write out 6 completely different reactions of eyclopentanone (reagent, product b) Write out 3 preparations of 3-methyl-1-butanol, a different starting material for each one. In some preps you just have to change the functional group, in other preps you may have to construct the carbon chain. c) Write out 3 preparations of 3-methylbutangle acid, a different starting material for each one. In some...

  • 9. Write out the mechanism for: MACN > Sw2 10. a) Write out 6 completely different...

    9. Write out the mechanism for: MACN > Sw2 10. a) Write out 6 completely different reactions of 3-hexanone (reagent, product). b) Write out 3 preparations of 3-phenyl-1-propanol, a different starting material for each one. In some preps you just have to change the functional groups in other props you may have to construct the carbon chain. c) Write out 3 preparations of hexanoic acid, a different starting material for cach one. In some preps you just have to change...

  • 1151 VCL 11-8: Claisen Condensation -1 For this assignment, the target compound that you should s...

    1151 VCL 11-8: Claisen Condensation -1 For this assignment, the target compound that you should synthesize is methyl acetoacetate. This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep in mind the mechanism and that you need to acidify the intermediate in order to isolate a neutral product. Synthesis Procedures 1. Start Virtual ChemLab and select Claisen Condensation-I from the list of assignments in the electronic workbook. After...

  • please dont miss the questions 11-4: Aldol - 1 For this assignment, the target compound that...

    please dont miss the questions 11-4: Aldol - 1 For this assignment, the target compound that you should synthesize is 2-ethyl-3-hydroxy-hexanal. This is a symmetric aldol reaction. Examine the product and determine which bond may be formed to link the two aldehydes. Keep in mind the mechanism and identify the nucleophile and the electrophile. Synthesis Procedures 1. Start Virtual ChemLab and select Aldol – 1 from the list of assignments on the whiteboard. After entering the synthesis laboratory, use the...

  • PLEASE ANSWER QUESTIONS 8-10 PLEASE ANSWER # 8-10!!!! Your goal for this experiment is to design...

    PLEASE ANSWER QUESTIONS 8-10 PLEASE ANSWER # 8-10!!!! Your goal for this experiment is to design a synthesis for: o- Experiment Questions How do I design a multi-step syntheses given starting material and product? • How can I synthesize trans-1,2-cyclohexanediol from hexanol using reactions already learned in lecture and lab? Experiment Techniques · Using distillation as a separation technique. • Using washing (a type of extraction) for purification Introduction So far this semester, you have performed three different types of...

  • NMR IR CAN YOU PLEASE ANSWER AS SOON AS POSSIBLE THANK YOU PLEASE EXPLAIN IT IN DETAIL THANK YOU Experimental Data Only report the IR absorptions that provide diagnosis...

    NMR IR CAN YOU PLEASE ANSWER AS SOON AS POSSIBLE THANK YOU PLEASE EXPLAIN IT IN DETAIL THANK YOU Experimental Data Only report the IR absorptions that provide diagnosis for the major functional groups. Copies of your spectra will be included in your lab report with this information written on the spectra. However, the information should also be included in the body of the report in a text format similar to the example given below IR cm1: 1735 (C-o); MS:...

  • can you please show the work.. thank you in Black New Tab MyUn Sign in Learn...

    can you please show the work.. thank you in Black New Tab MyUn Sign in Learn @ cheggc GetH Mic x Sign .pdf 1) Choose one molecule from the set and create an 8-step synthesis scheme using the chosen molecule as your starting material. You need to write the complete set of reagents and draw the product expected from each step. Reagents typically used together are considered one step, e.g. 1) LAH 2) H20 should be considered as one step....

  • Please show any work or explanation and help with filling out the data table. I appreciate...

    Please show any work or explanation and help with filling out the data table. I appreciate it very much. Thank you! 5. (Opts) Propose opts) Propose a reasonable to heterostom for the organic molecule that gave rise to the spectra below. Complete the me poctra below. Complete the datablas below related to the structure that you've identified Mass Spectrum 100 Relative Intensity 10 20 30 40 50 70 80 90 60 m/z 100 110 IR Spectrum 028 1936.93 13C NMR...

  • Synthesis of 1-Bromobutane: An SN2 Reaction Pre-Laboratory Exercises PRE-LABORATORY EXERCISES NAME: Cynthesis of 1-Bromobutane: An SN...

    Synthesis of 1-Bromobutane: An SN2 Reaction Pre-Laboratory Exercises PRE-LABORATORY EXERCISES NAME: Cynthesis of 1-Bromobutane: An SN 2 Reaction Butylbromide was prepared by refluxing in a 100-ml round bottomed flask a solution containing 13:35 Br 15 ml of water, 10 mL of n-butyl alcohol. 15 ml of concentrated H.SO. and a few boiling stories, 1. 2. R." d 1.275 laborales Nel CH3CH2CH2CH2OH + NaBr H2SO4 Superletalyst CHCH2CH2CHBr + NaHSO + HO (eq. 16) 1-butanol bp 118 C 1-bromobutane d 0.810 bp...

  • need help with the boxed bullet point. writing the chemical reaction scheme for the experiment. Synthesis of an A...

    need help with the boxed bullet point. writing the chemical reaction scheme for the experiment. Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...

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