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Chapter 9: Problem 24

a. Identify the protons with different chemical shifts in each of the structures shown. Use letter subscripts \(\mathrm{H}_{A}, \mathrm{H}_{B}\), and so on, to designate nonequivalent protons. Use models if necessary. (i) cis- and trans-2-butene (ii) 1,3-butadiene (iii) 1 -chloro-2,2-dimethylbutane (iv) 2-butanol (v) trans-1,2-dibromocyclopropane b.* Why does 3-methyl-2-butanol have three methyl resonances with different chemical shifts in its proton \(\mathrm{nmr}\) spectrum? c. \(^{*}\) For the compounds in Part a designated those protons (if any) that are enantiotopic or diastereotopic.

Short Answer

Expert verified
Protons have different shifts due to distinct structural environments.

Step by step solution

01

Analyze (i) Cis- and Trans-2-butene

In cis-2-butene, due to symmetry, both methyl groups will have er responses. Thus, it will have two sets of protons: - \(\mathrm{H}_A\): The protons in the terminal methyl groups.- \(\mathrm{H}_B\): The protons on the alkene carbon atom. In trans-2-butene, all four protons are in distinct environments. Therefore:- \(\mathrm{H}_A\): The protons in one methyl group.- \(\mathrm{H}_B\): The protons in the opposite methyl group.- Two distinct vinylic protons: \(\mathrm{H}_C\) and \(\mathrm{H}_D\). One on each alkene carbon atom.
02

Examine (ii) 1,3-Butadiene

The structure of 1,3-butadiene features different sets of proton environments:- \(\mathrm{H}_A\): Protons on the terminal carbon (C1/C4).- \(\mathrm{H}_B\): Protons on the central carbons (C2/C3).The geometric arrangement causes protons in each of these positions to experience different environments.
03

Consider (iii) 1-Chloro-2,2-dimethylbutane

This compound has distinct proton environments based on structure:- \(\mathrm{H}_A\): Protons of the terminal methyls (CH3 groups).- \(\mathrm{H}_B\): Protons on the methylene group attached to the chlorine (CH2).- \(\mathrm{H}_C\): Methyl protons farthest from the Cl group.
04

Identify (iv) 2-Butanol

In 2-butanol, protons are found in three sets based on environment:- \(\mathrm{H}_A\): The protons in two methyl groups.- \(\mathrm{H}_B\): The protons in the methylene group.- \(\mathrm{H}_C\): The single proton of the alcohol group (OH).- \(\mathrm{H}_D\): The unique proton at the chiral carbon.
05

Evaluate (v) Trans-1,2-dibromocyclopropane

This compound has three distinct proton environments:- \(\mathrm{H}_A\): The axial and equatorial protons of the cyclopropane ring related to each bromine (each set distinct due to stereochemistry).- \(\mathrm{H}_B\) and \(\mathrm{H}_C\): Axial and equatorial for each side.
06

Explain 3-Methyl-2-butanol

3-Methyl-2-butanol has three methyl groups; they are in different environments due to the molecule's geometry and sterics resulting from the chiral carbon center: - Each methyl group experiences different shielding/deshielding effects due to varying proximity to the hydroxyl group and substituents.
07

Designate Enantiotopic and Diastereotopic Protons (Part C)

Enantiotopic and diastereotopic distinguishability based on symmetry: - Enantiotopic: Protons in identical environments but different spatial orientations. - Diastereotopic: Protons in different environments because of stereochemistry Examples from given structures: - cis-2-butene has potentially enantiotopic vinylic hydrogens. - 1-Chloro-2,2-dimethylbutane's methylene protons are diastereotopic.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Proton Chemical Shift
Proton Chemical Shift is a crucial concept in NMR Spectroscopy that allows us to understand the different environments surrounding hydrogen nuclei in a molecule. When a compound is placed in a magnetic field, the protons resonate at different frequencies depending on their chemical environment. This is known as the chemical shift, measured in parts per million (ppm). Various factors affect the chemical shift:
  • Electronegative atoms: Atoms like oxygen or chlorine withdraw electron density from nearby protons, causing a downfield shift (higher ppm).
  • Magnetic Anisotropy: Alkenes and aromatic rings create anisotropic environments causing shifts distinct from aliphatic hydrogens.
  • Hybridization: Different hybridizations (sp3, sp2, sp) influence chemical shift due to variation in s-character.
These variations are vital for identifying nonequivalent hydrogen atoms in compounds like cis- and trans-2-butene, where symmetry and electronic environment lead to diverse shifts.
Cis-Trans Isomerism
Cis-trans isomerism occurs when atoms or groups with the same connectivity differ in their spatial arrangement. This spatial difference leads to diverse physical and chemical properties, including different NMR shifts. Cis and trans isomers have different environments due to the position of functional groups relative to a double bond or a ring structure.
Using cis- and trans-2-butene as examples, we notice:
  • Cis isomers: Their similar groups are on the same side, leading to a more symmetrical environment and thus a similar set of chemical shifts.
  • Trans isomers: Groups are opposite, causing each proton group to experience a different magnetic environment, thus causing more differentiated chemical shifts.
Such differences are important to recognize when analyzing NMR data, as they determine the isomeric form of a compound.
Enantiotopic and Diastereotopic Protons
In molecules, some protons may appear identical but interact differently in chiral or stereochemically complex environments. This differentiation leads to the concepts of enantiotopic and diastereotopic protons.
  • Enantiotopic protons: Found in symmetrical structures, these protons are chemically equivalent but become non-equivalent in chiral environments. An example is the vinylic hydrogens in cis-2-butene, which can react or resonate differently when introduced into a chiral environment.
  • Diastereotopic protons: Naturally exist in different environments because of adjacent chiral centers affecting their chemical environment. For example, in 1-chloro-2,2-dimethylbutane, the methylene protons are diastereotopic due to the influence of the chlorine group's stereochemistry.
This distinction aids in interpreting NMR spectra, particularly in identifying the stereochemical landscape of organic molecules.
Symmetry in Organic Compounds
Symmetry plays a pivotal role in determining the chemical equivalence of protons in organic molecules. Compounds with high symmetry often show fewer distinct resonances because many protons are in the same environment. Conversely, asymmetrical compounds display a wider variety of chemical shifts.
  • High symmetry effect: In cis-2-butene, there is a degree of symmetry that leads to fewer distinct proton resonances compared to its trans counterpart.
  • Low symmetry effect: Compounds like 2-butanol, which have complex structures with different substituents (such as a hydroxyl group and variable carbon branching), show more distinct resonances as protons are in varied environments.
Understanding symmetry helps chemists predict and interpret NMR spectra, revealing how protons are arranged and which are equivalent or distinct.

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Most popular questions from this chapter

In reasonably concentrated solution in water, ethanoic acid (acetic acid) acts as a weak acid (less than \(1 \%\) dissociated). Ethanoic acid gives two proton nmr resonance lines at 2 and 11 ppm, relative to TMS, whereas water gives a line at \(5 \mathrm{ppm} .\) Nonetheless, mixtures of ethanoic acid and water are found to give only two lines. The position of one of these lines depends on the ethanoic acid concentration, whereas the other one does not. Explain how you would expect the position of the concentration-dependent line to change over the range of ethanoic acid concentrations from \(0-100 \%\).

a. Show how the assignment of \(J_{A B}=J_{B C}=2 J_{A C}\) leads to the prediction of four equally spaced and equally intense lines for the methyl resonance of 2 -phenylpropene. b. What would the splittings of the alkenic and methyl protons look like for trans-1-phenylpropene if \(J_{A B}=16 \mathrm{~Hz}\), \(J_{A C}=4 \mathrm{~Hz}\), and \(J_{B C}=0 \mathrm{~Hz} ?\)

Explain how a mass spectrometer, capable of distinguishing between ions with \(m / e\) values differing by one part in 50,000 , could be used to tell whether an ion of mass 29 is \(\mathrm{C}_{2} \mathrm{H}_{5}^{+}\) or \(\mathrm{CHO}^{+}\).

The mass spectrum of propylbenzene has a prominent peak at mass number 92. With (3,3,3trideuteriopropyl)benzene, this peak shifts to 93. Write a likely mechanism for breakdown of propylbenzene to give a fragment of mass number 92 .

a. Calculate the relative intensities of the \((\mathrm{M}+1)^{+}\) and \((\mathrm{M}+2)^{+}\) ions for a molecule of elemental composition \(\mathrm{C}_{3} \mathrm{H}_{7} \mathrm{NO}_{2}\) b. The \(\mathrm{M}^{+},(\mathrm{M}+1)^{+}\), and \((\mathrm{M}+2)^{+}\) ion intensities were measured as \(100,8.84\), and \(0.54\) respectively, and the molecular weight as 120 . What is the molecular formula of the compound? c. In our example of how natural \({ }^{13} \mathrm{C}\) can be used to determine the number of carbon atoms in a compound with \(\mathrm{M}^{+}=86\) and a \((\mathrm{M}+1)^{+} / \mathrm{M}^{+}\) ratio of \(6.6 / 100\), we neglected the possible contribution to the \((\mathrm{M}+1)^{+}\) peak of the hydrogen isotope of mass 2 (deuterium). The natural abundance of deuterium is \(0.015 \%\) For a compound of composition \(\mathrm{C}_{6} \mathrm{H}_{14}\), how much do you expect the deuterium to contribute to the intensity of the \((\mathrm{M}+1)^{+}\) peak relative to the \(\mathrm{M}^{+}\) peak?
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