Question

3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) CH2COH Cl b) Cl 4. Number these in order of ease of hydrolysis. 1 -easiest to hydrolyze, 4- hardest to hydrolyze. EN Cl
0 0
Add a comment Improve this question Transcribed image text
Answer #1

please rate. thank you.

Add a comment
Know the answer?
Add Answer to:
3. Show the steps necessary to transform the acid on the left into the compound on...
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
  • 2. Show the step(s) necessary to transform the compound on the left into the acid on...

    2. Show the step(s) necessary to transform the compound on the left into the acid on the right. HOCH CH CH Br + HOCH2CH2CH,COH 19 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) H2C=CHCH_COH – H.C-chch_Coch; H2C=CHCH COH H2C=CHCHÖNCHS CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. CH;CH&CI CH,CHUCNHC,H, NCCH, CHOCCH,

  • 3. Show the steps necessary to transform the acid on the left into the compound on...

    3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCI2 a) -CHCHOCH Р-снсн. Сон Н.С-СНСH,CoСНB Н-С-СНCH,COН несиси вусая, b) Н.С-СНСH,CоН нсснсн 2он Н,С-СНСH,CNСАНЯ CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 =easiest to hydrolyze, 4 hardest to hydrolyze. сHсн2нся. сновсм, CH2CH2CNHC&Hs CHоёсн, CH3CH2CCI N=CCH3

  • 1. Name these compounds: *) HOSCH.HCH o cuddChuquichs b) Na - PCHCHICH " CH CH.CH)ÇUCH сн;...

    1. Name these compounds: *) HOSCH.HCH o cuddChuquichs b) Na - PCHCHICH " CH CH.CH)ÇUCH сн; 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. 1-pentanol → pentanoic acid 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. pentanoic acid isopropyl pentanoate pentanoic acid N-phenylpentanamide 4. Number these in order of ease of hydrolysis. 1 - easiest...

  • 1. Name these compounds: 9 сн,сессн,дося, CH3C=CCH2COH b) CHÚC-CCH,lona* CH?C=CCHąČN(CH2CH_CH3)2 2. Show the step(s) ne...

    1. Name these compounds: 9 сн,сессн,дося, CH3C=CCH2COH b) CHÚC-CCH,lona* CH?C=CCHąČN(CH2CH_CH3)2 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. CH,C=COH CH3C=CCH2OH 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOC12. a) CH;C=CCH,COH - снсесснRocнск b) CH3C=CCH_COH » CHỤC=CCHCNCH) ber these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. O...

  • 1. Name this compound, including stereochemistry: НО CHCHCH,ОН 2. Show the step(s) necessary to transform the...

    1. Name this compound, including stereochemistry: НО CHCHCH,ОН 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. Benzyl alcohol benzoic acid 3. What are the products of the following reaction? H30 CHO OCH3 -

  • 1. Name this compound, including stereochemistry: НОС CoHs HOC 2. Show the step(s) necessary to transform...

    1. Name this compound, including stereochemistry: НОС CoHs HOC 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. Methoxybenzene p-methoxybenzoic acid 3. What are the products of the following reaction? OCH3 Н,о* OCH3

  • 1. Show how to transform the compound on the left into the compound on the right.

     1. Show how to transform the compound on the left into the compound on the right. Several steps will be involved. You may use any additional organic or inorganic compounds you wish.2. Draw all resonance contributors to this radical. If there are no others, write 'None".  3. Write in all the products of this reaction: 4. Label all carbons in this molecule as to whether they are 1°, 2° or 3° 5. Draw in all vinyl H's (if any) with the subscript 'v" this way: HyDraw...

  • 1. Name this compound, including stereochemistry: HOCCECCH,CH Show the step(s) necessary to transform the compound...

    1. Name this compound, including stereochemistry: HOCCECCH,CH Show the step(s) necessary to transform the compound on the left into the acid on the right. chlorobenzene benzoic acid 3. What are the products of the following reaction? H:0* 4. Write in the product of this reaction: H2O C6H5CH2C=N ------ H. heat 5. Which type of spectroscopy (IR, 'H NMR, and/or SC NMR) would be good to distinguish between acetonitrile and acetic acid? State what you would observe for each compound in...

  • Add curved arrows to show how the compound on the left is converted to the compound...

    Add curved arrows to show how the compound on the left is converted to the compound on the right. Squaric acid has a pKa of 1.5, making it much more acidic than many carboxylic acids (typical pKa values of 4-5). One of the reasons for its acidity is resonance stabilization of its conjugate base. which is shown below. Add curved arrows to the structure on the left to show how it is converted to the other resonance contributor shown to...

  • Show the detailed synthesis of the following compound from but-1-ene. Show the steps in the correct...

    Show the detailed synthesis of the following compound from but-1-ene. Show the steps in the correct order, with numbers identifying the steps, the necessary conditions and showing intermediate reaction structures. It is not necessary to show the reaction mechanism. Н.С нс- -ОН

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