A compound shows strong, very broad IR absorption in the region 3300-3600 cm¹ and strong, sharp absorption at 1715 cm ¹. What functional group accounts for both of these absorptions? (Select all that apply.) 0-Halcohol C-Hocarboxylic acid C=Cester C=Oether C-Oketone Submit Answer Retry Entire Group 8 more group attempts remaining

A compound shows strong, very broad IR absorption in the region 3300-3600 cm¹ and strong, sharp absorption at 1715 cm ¹. What functional group accounts for both of these absorptions? (Select all that apply.) 0-Halcohol C-Hocarboxylic acid C=Cester C=Oether C-Oketone Submit Answer Retry Entire Group 8 more group attempts remaining

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Please correct answer and don't use hand rating
Draw the structure of molecule
How many kinds of chemically non-equivalent hydrogens are there in each of the following compounds? CH H он Ibuprofin, active enantiomer (ant-inflamatory) a The number of chemically non-equivalent hydrogens is он CH2 Aspirin (analgesic, antipyretic and antibiotic) b The number of chemically non-equivalent hydrogens is 5 Submit Answer Retry Entire Group 8 more group attempts remaining
Identify each peak (peak splitting and ppm) and identify the unknown compound. Please draw the structure, and explain why its that structure. Attached are the spectra for the unknown compound.
The proton nmr is 1H Septet between 3.5 and 4 3H singlet at about 3.4 6H doublet at about 1.2
What change in the IR spectrum is consistent with the reaction below? SOCI₂ / Pyr OH CI a) Two new absorptions should appear at 3200-3600 cm-¹ b) A new absorption should appear at 2950 cm-¹ c) A new absorption should appear at 3200-3600 cm ¹¹ d) An absorption at 3200-3600 cm³¹ should disappear
1. Which of the following compound will show two absorption bands at around 2700 cm³¹ and around 2800 cm¹ along with the carbonyl absorption [Select] 4 Click here to preview the image B :0: A A CO :0: lg i l N B C 2. Which of the following compound will show absorption band ~3300 cm¹ [Select] Click here to preview image A B B D C H 3. Which the following compound will show absorption band ~1735 cm1 [Select] Click here to preview image e D NH
Please solve I'll rate for it
Provide detail analysis conclusion for the Qualitative Tests for carbonyls and Unknown Carbonyl.
Which of the following statements are true regarding the following compound? (Select all apply, Points will be deducted for incorrect answers) O NH₂ This compound shows m/z 43 fragment in mass spectrum In broad band decoupled 13C NMR spectrum, this compound shows 11 signals IR spectrum shows a strong peak around 1715 cm-1 In ¹H NMR spectrum, this compound shows 6 signals IR spectrum shows a moderate, sharp peak around 1600 cm-¹ The compound shows a peak above 200 nm in UV-visible spectrum IR spectrum shows a moderate, sharp peak around 2230 cm! H
Problem 8 114 IR Spectrum (quid fim) 4000 3000 2000 1600 1200 V (cm') 800 100 80 Mass Spectrum 57 More branch 60 E Co M 114 ( 1%) No significant UV 40 absorption above 220 nm 20 99 CBH18 2メ8k8-み8) 16 18-(6) 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50 O MHz. CDCI, solution) DEPT CH, CH,t CHt KAS ASym. 1500 solvent proton decoupled CAl3 Sym o 8(ppm) 340 200 160 120 80 40 1H NMR Spectrum (200 MHz. CDCIg solution) TMS 2 8. 7 6. 5 4 8 (ppm) 10 Sof base peak
I'm having a hard time distinguishing what functional group that broad peak is because it seems to spill over into all of them bc its so wide. can someone explain?