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Question

The $^{19}F$ NMR spectrum of $SF_4$ consists of:

The correct answer is
Two 1:2:1 triplets of equal intensity

Understanding the $SF_4$ $^{19}F$ NMR Spectrum

The question asks about the nature of the $^{19}F$ Nuclear Magnetic Resonance ($^{19}F$ NMR) spectrum for the molecule sulfur tetrafluoride ($SF_4$). To determine this, we need to consider the structure of $SF_4$ and the principles of NMR spectroscopy.

Molecular Structure of $SF_4$

Sulfur tetrafluoride ($SF_4$) has a central sulfur atom bonded to four fluorine atoms. Due to the presence of a lone pair of electrons on the sulfur atom, the molecule adopts a seesaw molecular geometry. This geometry arises from a trigonal bipyramidal electron geometry.

  • In the seesaw structure, there are two distinct types of positions for the fluorine atoms:
  • Two axial fluorine atoms (let's denote them as Fa).
  • Two equatorial fluorine atoms (let's denote them as Fe).

Importantly, the axial and equatorial fluorine atoms are not chemically equivalent due to the constraints of the seesaw geometry.

NMR Spectroscopy Principles

In NMR spectroscopy, signals from magnetically equivalent nuclei are identical. However, signals from non-equivalent nuclei appear at different chemical shifts. Furthermore, nuclei can interact with neighboring non-equivalent nuclei through spin-spin coupling, which causes the signals to split into multiple peaks (multiplicity).

  • The splitting pattern depends on the number and type of neighboring nuclei.
  • For spin 1/2 nuclei (like $^{19}F$), coupling to $n$ equivalent neighboring nuclei typically results in a multiplet with $n+1$ peaks.
  • The relative intensities of these peaks follow Pascal's triangle. For example:
    • Coupling to 1 nucleus: Doublet (1:1 intensity)
    • Coupling to 2 equivalent nuclei: Triplet (1:2:1 intensity)

Predicting the $^{19}F$ NMR Spectrum of $SF_4$

Considering the two types of fluorine atoms in $SF_4$:

  • Axial Fluorines (Fa): Each axial fluorine atom experiences coupling with the two equatorial fluorine atoms. Since the two equatorial fluorine atoms (Fe) are equivalent to each other, each Fa atom experiences coupling to a system equivalent to a single nucleus with spin $I=1$ (since two spin 1/2 nuclei coupled together have a resultant spin state of 0 or 1). This interaction causes the signal for the axial fluorines to split into a triplet with relative intensities of 1:2:1.
  • Equatorial Fluorines (Fe): Similarly, each equatorial fluorine atom experiences coupling with the two axial fluorine atoms. Since the two axial fluorine atoms (Fa) are equivalent to each other, each Fe atom experiences coupling to a system equivalent to a single nucleus with spin $I=1$. This interaction causes the signal for the equatorial fluorines to split into a triplet with relative intensities of 1:2:1.

Because there are two distinct types of fluorine atoms (axial and equatorial), we expect to observe two separate signals in the $^{19}F$ NMR spectrum.

Each of these signals is a triplet with 1:2:1 intensity.

Since there are two axial fluorines contributing to one signal and two equatorial fluorines contributing to the other signal, and these groups are electronically similar in terms of their coupling interactions leading to the triplet, the overall intensities of these two distinct triplets are expected to be equal.

Conclusion

Therefore, the $^{19}F$ NMR spectrum of $SF_4$ consists of two distinct signals, each split into a triplet (1:2:1 intensity), and these two triplets have equal overall intensity.

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Important Questions from 1h NMR and 13c NMR Spectroscopy

  1. In an 1H-NMR spectra three samples were examined. One being pure acetic acid, other one pure water and a 1 : 1 mixture of acetic acid and water. The number of peaks formed for each sample would be _________, _________, ____________.

  2. The [(η5-C5H5)Fe(CO)2]2 molecule exists in solution as a 1 : 1 mixture of cis- and trans-isomers.
    At 28°C, 1H NMR spectrum of the molecule shows

  3. The correct match for the molecules given in Column P with the spectral data given in Column Q is

    Column PColumn Q
    A.Ethyl acetatei.Two singlets in 1H NMR
    B.2-chloropentaneii.Peak intensity at M:(M+2) is 3:1 in EI-MS
    C.1,2-dibromo-2-methylpropaneiii.Absorption band at 1740 cm-1 in IR
  4. The natural product that gives a signal at δ 218 ppm in its 13C NMR spectrum is

  5. The 1H NMR spectrum of a mixture of chloroform and acetone shows two singlets at δ7.25 and 2.1 ppm with integral heights of 12 and 18 mm, respectively. The molar ratio of chloroform to acetone in the mixture is

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