/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Q2P Question: The \(^{\bf{1}}{\bf{H}... [FREE SOLUTION] | 91Ó°ÊÓ

91Ó°ÊÓ

Question: The \(^{\bf{1}}{\bf{H}}\) NMR spectrum 1,2-dimethoxyethane \(\left( {{\bf{C}}{{\bf{H}}_{\bf{3}}}{\bf{OC}}{{\bf{H}}_{\bf{2}}}{\bf{C}}{{\bf{H}}_{\bf{2}}}{\bf{OC}}{{\bf{H}}_{\bf{3}}}} \right)\) recorded on a 300 MHz NMR spectrometer consists of signals at 1017 Hz and 1065 Hz downfield from TMS. (a) Calculate the chemical shift of each absorption. (b) At what frequency would each absorption occur if the spectrum were recorded on a 500 MHz NMR spectrometer?

Short Answer

Expert verified

a) The chemical shifts for signals at 1017 Hz and 1065 Hz are 3.39 ppm and 3.55 ppm, respectively.

(b) The absorbed frequencies for 3.39 ppm and 3.55 ppm are 1695 Hz and 1775 Hz, respectively

Step by step solution

01

Chemical shift formula

The formula for the chemical shift is given as follows:

\({\bf{\delta = }}\frac{{{\bf{Absorbed}}\;{\bf{frequency}}\left( {{\bf{Hz}}} \right)}}{{{\bf{Frequency}}\;{\bf{of}}\;{\bf{the}}\;{\bf{operator}}\left( {{\bf{MHz}}} \right)}}\)

02

Calculation of chemical shift in a

(a)The frequency of the NMR spectrometer is 300 MHz.

The signals are 1017 Hz and 1065 Hz. Substitute the values in the above formula.

\(\begin{array}{c}{\rm{Chemical}}\;{\rm{shift}} = \frac{{{\rm{1017}}\;{\rm{Hz}}}}{{{\rm{300}}\;{\rm{MHz}}}}\\{\rm{\delta }} = 3.39\;{\rm{ppm}}\\\\{\rm{Chemical}}\;{\rm{shift}} = \frac{{{\rm{1065}}\;{\rm{Hz}}}}{{{\rm{300}}\;{\rm{MHz}}}}\\{\rm{\delta }} = 3.55\;{\rm{ppm}}\end{array}\)

Thus, the chemical shifts for signals at 1017 Hz and 1065 Hz are 3.39 ppm and 3.55 ppm, respectively.

03

Calculation for b

(b) The chemical shifts forsignals at 1017 Hz and 1065 Hzare 3.39 ppm and 3.55 ppm, respectively. Thefrequency of the NMR spectrometer is 500 MHz.

The absorbed frequency for 3.39 ppm is calculated as follows:

\(\begin{array}{c}{\rm{\delta }} = \frac{{{\rm{Absorption}}\;{\rm{frequency}}}}{{{\rm{500}}\;{\rm{MHz}}}}\\3.39\;{\rm{ppm}} = \frac{{{\rm{Absorption}}\;{\rm{frequency}}}}{{{\rm{500}}\;{\rm{MHz}}}}\\{\rm{Absorption}}\;{\rm{frequency}} = 3.39\;{\rm{ppm}}\left( {{\rm{500}}\;{\rm{MHz}}} \right)\\ = 1695\;{\rm{Hz}}\end{array}\)

The absorbed frequency for 3.55 ppm is calculated as follows:

\(\begin{array}{c}{\rm{\delta }} = \frac{{{\rm{Absorption}}\;{\rm{frequency}}}}{{{\rm{500}}\;{\rm{MHz}}}}\\3.55\;{\rm{ppm}} = \frac{{{\rm{Absorption}}\;{\rm{frequency}}}}{{{\rm{500}}\;{\rm{MHz}}}}\\{\rm{Absorption}}\;{\rm{frequency}} = 3.55\;{\rm{ppm}}\left( {{\rm{500}}\;{\rm{MHz}}} \right)\\ = 1775\;{\rm{Hz}}\end{array}\)

Thus, the absorbed frequencies for 3.39 ppm and 3.55 ppm are 1695 Hz and 1775 Hz, respectively.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91Ó°ÊÓ!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

How many lines are observed in the \({}^{{\bf{13}}}{\bf{C}}\) NMR spectrum of each compound?

a.

b.

c.

d.

Draw all constitutional isomers of molecular formula \({{\bf{C}}_{\bf{3}}}{{\bf{H}}_{\bf{6}}}{\bf{C}}{{\bf{l}}_{\bf{2}}}\).

a. How many signals does each isomer exhibit in its \({}^{\bf{1}}{\bf{H}}\) NMR spectrum?

b. How many lines does each isomer exhibit in its \({}^{{\bf{13}}}{\bf{C}}\) NMR spectrum?

c. When only the number of signals in both \({}^{\bf{1}}{\bf{H}}\) and \({}^{{\bf{13}}}{\bf{C}}\) NMR spectroscopy is considered, is it possible to distinguish all of these constitutional isomers?

How many peaks are observed in the 1HNMR signal for each proton shown in red in palau'amine, the complex chapter-opening molecule?

The 1H NMR spectrum of CH3OH recorded on a 500 MHz NMR spectrometer consists of two signals, one due to the CH3 protons at 1715 Hz and one due to the OH proton at 1830 Hz, both measured downfield from TMS. (a) Calculate the chemical shift of each absorption. (b) Do the CH3 protons absorb upfield or downfield from the OH proton?

Question: Propose a structure consistent with each set of data.

a. A compound X (molecular formula C6H12O2) gives a strong peak in its IR spectrum at 1740 cm-1. The 1 H NMR spectrum of X shows only two singlets, including one at 3.5 ppm. The 13C NMR spectrum is given below Propose a structure for X.

b. A compound Y (molecular formula C6H10 ) gives four lines in its 13C NMR spectrum (27, 30, 67, and 93 ppm), and the IR spectrum given here. Propose a structure for Y.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.