Please correct answer and don't use hand rating and don't use Ai solution Predict the functional group corresponding to an IR spectrum with described peaks.A strong peak around 1700-1725 cm and broad peaks around 2500-3300 cm Choose...-1 Choose...A single strong peak around 1705-1725 cmStrong peaks around 1000-1300 cm Choose...A strong peak around 1735-1750 cm and strong peaks around 1000-1300 cm Choose...

Based on the infrared (IR) spectrum peaks described in the image, here are the typical functional…

Answered: Predict the functional group…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterL4: Proton (1h) Nmr Spectroscopy

Section: Chapter Questions

Problem 21CTQ

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Assign each peak on the following spectrum.
Please solve correctly, with some explanation too. (Gpt/ai wrong answer not allowed)
Match the peaks in this spectrum with hydrogens on the structure below. A) H3C I H₂ 3.0 H₂ CH3 IV 2.0 ppm 1.0 1.68 ppm II: 0.99 ppm III: 2.32 ppm IV: 3.61 ppm 1: B) I: 0.99 ppm II: 1.68 ppm III: 2.32 ppm IV: 3.61 ppm C) I: II: 1.68 ppm 0.99 ppm +
Acetyleugnol: Match the peaks to the appropriate number on the structure.
For each pair of compounds, select the one that best fits the given spectral data.
A.) How many signals are seen for the CNMR spectrum of the unknowns C6H14O? B.) Explain the chemical shifts of the signals seen based upon the location of the carbons that are relative to deshielding group if any are seen in the compound (unknown is C6H14O)? For question A. I believe it is 4 signals. For question B. I know that none of the signals are in the deshielding are of the chart but are all located in the shielded region but i am unsure of how to determine the chemical shifts of the given signal. If possible an in-depth explanation would be greatly appreciated in order to understand this better.
Identify the following spectra. Assign all pertinent peaks (~5-6 peaks). Place the structure of the compound in the box on the lower left-hand corner of spectrum. .
Please label the peaks appropriately. Draw the structure on the spectra and label which peaks belong to which hydrogen. Include a spectroscopic analysis section describing each peak.
NEED HELP NOT GRADED PRACTICE
A.) How many signals does the HNMR of the unknown C6H14O have? B.)Whats the ratio between the number of different hydrogens in the unknown compound C6H14O? C.)Explain splitting patterns of all the signals (in depth if possible the lecture confused me). D.)Explain the chemical shifts of the signals based upon the locations of hydrogens relative to the desheilding groups if any are present in the compound. For A. I think there are 4 signals. For B. I think the ratio is 1:1:3:9 for the hydrogens on the HNMR spectrum. For the last 2 questions (C. and D.) the lecture confused me so an in depth of how you found the answer would be greatly appreciated. Also the unknown for the attached HNMR is C6H14O.
help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working
Using a 300 MHz NMR instrument:a. How many Hz downfield from TMS is a signal at 2.5 ppm?b. If a signal comes at 1200 Hz downeld from TMS, at what ppm does it occur?c. If two signals are separated by 2 ppm, how many Hz does this correspond to?

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