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Question: For each compound, first label each different type of proton and then rank the protons in order of increasing chemical shift.

a.

b.

c.

Short Answer

Expert verified

a.

b.

c.

Step by step solution

01

NMR spectroscopy

The chemical shift of the proton depends upon the atoms attached to it. The proton near the electronegative goes downshield or has more value of the chemical shift.

02

Explanation

a.

The given compound has three types of proton, as shown below:

Given compound in a

Cl is more electronegative than Br. Thus, the proton near Cl is more downshield as compared to the proton near Br.

The order of the chemical shft is shown below:

\({{\rm{H}}_{\rm{b}}} < {{\rm{H}}_{\rm{c}}} < {{\rm{H}}_{\rm{a}}}\)

b.

The given compound has three types of proton, as shown below:

Given compound in b

The proton between the oxygen atoms will go more downshield as compared to the proton near the oxygen atom at the extreme left.

The order of the chemical shft is shown below:

\({{\rm{H}}_{\rm{c}}} < {{\rm{H}}_{\rm{a}}} < {{\rm{H}}_{\rm{b}}}\)

c.

The given compound has three types of proton, as shown below:

Given compound in c

Proton near the oxygen atom will go more downshield as compared to the proton away from the oxygen atom.

The order of chemical shft is shown below:

\({{\rm{H}}_{\rm{c}}} < {{\rm{H}}_{\rm{a}}} < {{\rm{H}}_{\rm{b}}}\)

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Most popular questions from this chapter

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

Identify the carbon atoms that give rise to the signals in the \)^{{\bf{13}}}{\bf{C}}\) NMR spectrum of each compound.

a. \){\bf{C}}{{\bf{H}}_{\bf{3}}}{\bf{C}}{{\bf{H}}_{\bf{2}}}{\bf{C}}{{\bf{H}}_{\bf{2}}}{\bf{C}}{{\bf{H}}_{\bf{2}}}{\bf{OH}}\); \)^{{\bf{13}}}{\bf{C}}\) NMR: 14, 19, 35, and 62 ppm

b. \){\left( {{\bf{C}}{{\bf{H}}_{\bf{3}}}} \right)_{\bf{2}}}{\bf{CHCHO}}\); \)^{{\bf{13}}}{\bf{C}}\) NMR: 16, 41, and 205 ppm

c. \){\bf{C}}{{\bf{H}}_{\bf{2}}}{\bf{ = CHCH}}\left( {{\bf{OH}}} \right){\bf{C}}{{\bf{H}}_{\bf{3}}}\); \)^{{\bf{13}}}{\bf{C}}\) NMR: 23, 69, 113, and 143 ppm

Question: (a) How many 1H NMR signals does each compound show? (b) Into how many peaks is each signal split?

Propose a structure consistent with each set of data.

a. C9H10O2: IR absorption at 1718cm-1

b. C9H12 : IR absorption at 2850โ€“3150cm-1

Label each statement as True or False.

a. When a nucleus is strongly shielded, the effective field is larger than the applied field and the absorption shifts downfield.

b. When a nucleus is strongly shielded, the effective field is smaller than the applied field and the absorption is shifted upfield.

c. A nucleus that is strongly deshielded requires a lower field strength for resonance.

d. A nucleus that is strongly shielded absorbs at a larger ฮด value.

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