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Chapter 14: Q.21558-14-3P. (page 533)

How many 1H NMR signals does each compound show?

a.

b.

c.

d.

e.

f.

g.

h.

Short Answer

Expert verified

a. 2

b. 2

c. 2

d. 2

e. 4

f. 4

g. 5

h. 4

Step by step solution

01

NMR spectroscopy

Different types of proton NMR signals are observed in compounds due to the presence of different protons. The environment of these protons is affected by electron-withdrawing and electron-releasing groups.

02

 1H NMR signals in a, b, c, and d

a. The given compound has a plane of symmetry, as shown.

Plane of symmetry in a

Thus, the given compound has two types of protons, and it will give two signals.

b. The given compound has a plane of symmetry, as shown.

Plane of symmetry in b

Thus, the given compound has two types of protons, and it will give two signals.

c. The given compound has a plane of symmetry, as shown.

Plane of symmetry in c

Thus, the given compound has two types of protons, and it will give two signals.

d. The given compound has a plane of symmetry, as shown.

Plane of symmetry in d

Thus, the given compound has two types of protons, and it will give two signals.

03

 1H NMR signals in e, f, g and h

e. The given compound has four types of protons, and it will give four signals.

Structure of e

f. The given compound has four types of protons, and it will give four signals.

Structure of f

g. The given compound has five types of protons, and it will give five signals.

Structure of g

h. The given compound has four types of protons, and it will give four signals.

Structure of h

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Most popular questions from this chapter

Question: Cyclohex-2-enone has two protons on its carbon-carbon double bond (labeled Ha and Hb ) and two protons on the carbon adjacent to the double bond (labeled Hc ). (a) If Jab = 11 Hz and Jbc = 4 Hz, sketch the splitting pattern observed for each proton on the hybridized carbons. (b) Despite the fact that Ha is located adjacent to an electron-withdrawing C=O, its absorption occurs up-field from the signal due to Hb(6.0 vs. 7.0 ppm). Offer an explanation.

How can you use \(^{\bf{1}}{\bf{H}}\) NMR spectroscopy to distinguish between \({\bf{C}}{{\bf{H}}_{\bf{2}}}{\bf{ = C}}\left( {{\bf{Br}}} \right){\bf{C}}{{\bf{O}}_{\bf{2}}}{\bf{C}}{{\bf{H}}_{\bf{3}}}\)and methyl (E)-3-bromopropenoate, \({\bf{BrCH = CHC}}{{\bf{O}}_{\bf{2}}}{\bf{C}}{{\bf{H}}_{\bf{3}}}\)?

Question: The \(^{\bf{1}}{\bf{H}}\) NMR spectrum of \({\bf{C}}{{\bf{H}}_{\bf{3}}}{\bf{OH}}\) recorded on a 500 MHz NMR spectrometer consists of two signals, one due to the \({\bf{C}}{{\bf{H}}_{\bf{3}}}\) 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 \({\bf{C}}{{\bf{H}}_{\bf{3}}}\) protons absorb upfield or downfield from the OH proton?

Question: 18-Annulene shows two signals in its 1 H NMR spectrum, one at 8.9 (12 H) and one at –1.8 (6 H) ppm. Using a similar argument to that offered for the chemical shift of benzene protons, explain why both shielded and deshielded values are observed for 18-annulene.

Question: What effect does increasing the operating frequency of a1HNMR spectrum have on each value: (a) the chemical shift inδ ;(b) the frequency of an absorption in Hz; (c) the magnitude of a coupling constant J in Hz?

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