Question 4. You are asked to identify an unknown compound, which has the following analytical data: PPM Chemical Shift Integration 1 Multiplicity 8.28 7.95 1 d 7.48 1 6.99 4.11 1 d. 2 2.81 1.34 3 The peak at 8.28 ppm is found to disappear when the NMR sample is treated with

Within each set, can 'H NMR spectroscopy be used to differentiate between the two compounds? Briefly explain why or why not. Predict the 'H NMR spectrum for each compound (include integration, multiplicity, and approximate chemical shift). Either draw the actual spectrum or put in a data table format.

on 19 of 42 > Learning Loudon Parise SEVENTH EDITION Construct a simulated ¹H NMR spectrum, including proton integrations, for CH₂ OC(CH₂OCH (see Hint). Drag the appropriate splitting patterns to the approximate chemical shift positions; place the integration values in the small bins above the associated chemical shift. Splitting patterns and integrations may be used more than once, or not at all, as needed. Likewise, some bins might remain blank. Note that peak heights are arbitrary and do not indicate proton integrations. 30円 $ 4 R F V 7 % 5 T G B ^ 6 2H -Fo Y H MacBook Air & 7 RAM N 4 U Answer Bank J * 00 M 9H I ( 9 K ➤➤ 2 O < H ) O L 6H command P -3H sented by Macmillan Learning ^ 11 ; 0 ppm 95 { + 11 alt ? option } (1)

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