ZuoTi.Pro
Question
Please help. Thanks

Molecule A undergoes a Wolff-Kishner reaction to yield 2-methyipentane Use the H M provided for molecule A to determine its structure Molecule A Singlet, 3H Doublet, 6H Doublet, 2H Multiplet, IH PPM Extra credit: Deoxyribose is the sugar used in DNA (structure below). Draw the product that results from treating the cyclic hemiacetal with acid. OH H30 H,O но
science   chemistry   
0 0
Add a comment Improve this question Transcribed image text
Next > < Previous
Sort answers by oldest

Homework Answers

Answer #1

ts a aductron Wolff-kishnes-teachon Conveit nto an akane H C 3 сп 2 The nydoges a fashon () Shon Singlet near 2 ppm The h 1d,oger a产4ubl, n (3) Shu doublet, and equiv%Indt and . Show doublet-n ea 1 kisner

0 0
Add a comment
Know the answer?
Add Answer to:
Please help. Thanks Molecule A undergoes a Wolff-Kishner reaction to yield 2-methyipentane Use the H M...
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

  • 2. Use the 'H NMR and IR data to determine the structure of the following compounds...

    2. Use the 'H NMR and IR data to determine the structure of the following compounds and name them. Compound A Molecular formula: CroH IR absorptions at N/A H NMR data: 1.3 (singlet, 9H), 7.0 to 7.5 (multiplet, 5H) ppm Compound B Molecular formula: CHO IR absorptions at 1H NMR data: 1735-1745, 1050 cm 0.93 (doublet, 6H), 1.52 (multiplet, 2H), 1.69 (multiplet, 1H), 2.04 (singlet, 3H), and 4.10 (triplet,2H) ppm Compound C Molecular ion: IR absorptions at 1710 cm 1H...

  • Molecule C: Molecule D: Can someone PLEASE EXPLAIN the answers?????? 2. Below are the 'H and...

    Molecule C: Molecule D: Can someone PLEASE EXPLAIN the answers?????? 2. Below are the 'H and 13C NMR spectra for four isomers of C&H:02. Provide the structure that produced each set of spectra. Molecule A: 'H NMR 3H 3H no coupling, so no adjacent carbons with hydrogen atoms 2H 5 3 2 0 PPM 13C NMR aldehyde or ketone no aldehyde in 1H NMR, SO ketone 220 200 180 160 140 120 100 PPM 80 60 40 20 0 Molecule...

  • Please draw the unknown molecule presented in the specs, Thanks!!! Mass Spectrum (not shown): [M] = 169 (100%) m/z IR S...

    Please draw the unknown molecule presented in the specs, Thanks!!! Mass Spectrum (not shown): [M] = 169 (100%) m/z IR Spectrum (not shown): 2985, 2250 (m), 1745 cm1 (all listed are strong (s) unless otherwise indicated) H NMR Spectrum (400 MHz, CDC I3, 25 °C) 5 3 PPM 2H 2H 2H 6H 3H C NMR Spectrum (with DEPT), proton-decoupled (125 MHz, CDCI3, 25 °C) (CH2) (C) (CH3) (CH2) (CH3) (C) (C) (CH2) 180 160 80 140 120 100 PPM 60...

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