Concept explainers
(a)
Interpretation:
Protons in the given compound that gives the signal at the lowest frequency ‘a’, at the next lowest ‘b’ and so on has to be labelled.
Concept introduction:
Depending upon the electron density or the concentration of electron around the proton the chemical shift values of the proton varies relative to the reference signal.
The more the shielded proton less will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region.
The more the deshielded or less shielded proton more will be its chemical shift value and the corresponding signal will be produced at the left-hand side or higher frequency region.
Proton or set of proton attached near to the more electronegative or electron withdrawing atoms is more deshielded or less shielded and vice versa.
Signal multiplicity: In proton NMR spectrum, protons may or may not be split into one or more peaks.
It is referred as singlet, doublet, triplet, quartet, pentet, and multiplet.
The signal multiplicity is follow
(b)
Interpretation:
Protons in the given compound that gives the signal at the lowest frequency ‘a’, at the next lowest ‘b’ and so on has to be labelled.
Concept introduction:
Depending upon the electron density or the concentration of electron around the proton the chemical shift values of the proton varies relative to the reference signal.
The more the shielded proton less will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region.
The more the deshielded or less shielded proton more will be its chemical shift value and the corresponding signal will be produced at the left-hand side or higher frequency region.
Proton or set of proton attached near to the more electronegative or electron withdrawing atoms is more deshielded or less shielded and vice versa.
Signal multiplicity: In proton NMR spectrum, protons may or may not be split into one or more peaks.
It is referred as singlet, doublet, triplet, quartet, pentet, and multiplet.
The signal multiplicity is follow
(c)
Interpretation:
Protons in the given compound that gives the signal at the lowest frequency ‘a’, at the next lowest ‘b’ and so on has to be labelled.
Concept introduction:
Depending upon the electron density or the concentration of electron around the proton the chemical shift values of the proton varies relative to the reference signal.
The more the shielded proton less will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region.
The more the deshielded or less shielded proton more will be its chemical shift value and the corresponding signal will be produced at the left-hand side or higher frequency region.
Proton or set of proton attached near to the more electronegative or electron withdrawing atoms is more deshielded or less shielded and vice versa.
Signal multiplicity: In proton NMR spectrum, protons may or may not be split into one or more peaks.
It is referred as singlet, doublet, triplet, quartet, pentet, and multiplet.
The signal multiplicity is follow
(d)
Interpretation:
Protons in the given compound that gives the signal at the lowest frequency ‘a’, at the next lowest ‘b’ and so on has to be labelled.
Concept introduction:
Depending upon the electron density or the concentration of electron around the proton the chemical shift values of the proton varies relative to the reference signal.
The more the shielded proton less will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region.
The more the deshielded or less shielded proton more will be its chemical shift value and the corresponding signal will be produced at the left-hand side or higher frequency region.
Proton or set of proton attached near to the more electronegative or electron withdrawing atoms is more deshielded or less shielded and vice versa.
Signal multiplicity: In proton NMR spectrum, protons may or may not be split into one or more peaks.
It is referred as singlet, doublet, triplet, quartet, pentet, and multiplet.
The signal multiplicity is follow
(e)
Interpretation:
Protons in the given compound that gives the signal at the lowest frequency ‘a’, at the next lowest ‘b’ and so on has to be labelled.
Concept introduction:
Depending upon the electron density or the concentration of electron around the proton the chemical shift values of the proton varies relative to the reference signal.
The more the shielded proton less will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region.
The more the deshielded or less shielded proton more will be its chemical shift value and the corresponding signal will be produced at the left-hand side or higher frequency region.
Proton or set of proton attached near to the more electronegative or electron withdrawing atoms is more deshielded or less shielded and vice versa.
Signal multiplicity: In proton NMR spectrum, protons may or may not be split into one or more peaks.
It is referred as singlet, doublet, triplet, quartet, pentet, and multiplet.
The signal multiplicity is follow
(f)
Interpretation:
Protons in the given compound that gives the signal at the lowest frequency ‘a’, at the next lowest ‘b’ and so on has to be labelled.
Concept introduction:
Depending upon the electron density or the concentration of electron around the proton the chemical shift values of the proton varies relative to the reference signal.
The more the shielded proton less will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region.
The more the deshielded or less shielded proton more will be its chemical shift value and the corresponding signal will be produced at the left-hand side or higher frequency region.
Proton or set of proton attached near to the more electronegative or electron withdrawing atoms is more deshielded or less shielded and vice versa.
Signal multiplicity: In proton NMR spectrum, protons may or may not be split into one or more peaks.
It is referred as singlet, doublet, triplet, quartet, pentet, and multiplet.
The signal multiplicity is follow

Want to see the full answer?
Check out a sample textbook solution
Chapter 10 Solutions
EBK ESSENTIAL ORGANIC CHEMISTRY
- Michael Reactions 19.52 Draw the products from the following Michael addition reactions. 1. H&C CH (a) i 2. H₂O* (b) OEt (c) EtO H₂NEt (d) ΕΙΟ + 1. NaOEt 2. H₂O' H H 1. NaOEt 2. H₂O*arrow_forwardRank the labeled protons (Ha-Hd) in order of increasing acidity, starting with the least acidic. НОН НЬ OHd Онсarrow_forwardCan the target compound at right be efficiently synthesized in good yield from the unsubstituted benzene at left? ? starting material target If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area. Be sure you follow the standard ALEKS rules for submitting syntheses. + More... Note for advanced students: you may assume that you are using a large excess of benzene as your starting material. C :0 T Add/Remove step Garrow_forward
- The following equations represent the formation of compound MX. What is the AH for the electron affinity of X (g)? X₂ (g) → 2X (g) M (s) → M (g) M (g) M (g) + e- AH = 60 kJ/mol AH = 22 kJ/mol X (g) + e-X (g) M* (g) +X (g) → MX (s) AH = 118 kJ/mol AH = ? AH = -190 kJ/mol AH = -100 kJ/mol a) -80 kJ b) -30 kJ c) -20 kJ d) 20 kJ e) 156 kJarrow_forwardA covalent bond is the result of the a) b) c) d) e) overlap of two half-filled s orbitals overlap of a half-filled s orbital and a half-filled p orbital overlap of two half-filled p orbitals along their axes parallel overlap of two half-filled parallel p orbitals all of the abovearrow_forwardCan the target compound at right be efficiently synthesized in good yield from the unsubstituted benzene at left? starting material target If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area. Be sure you follow the standard ALEKS rules for submitting syntheses. + More... Note for advanced students: you may assume that you are using a large excess of benzene as your starting material. C T Add/Remove step X ноarrow_forward
- Which one of the following atoms should have the largest electron affinity? a) b) c) d) 으으 e) 1s² 2s² 2p6 3s¹ 1s² 2s² 2p5 1s² 2s² 2p 3s² 3p² 1s² 2s 2p 3s² 3p6 4s2 3ds 1s² 2s² 2p6arrow_forwardAll of the following are allowed energy levels except _. a) 3f b) 1s c) 3d d) 5p e) 6sarrow_forwardA student wants to make the following product in good yield from a single transformation step, starting from benzene. Add any organic reagents the student is missing on the left-hand side of the arrow, and any addition reagents that are necessary above or below the arrow. If this product can't be made in good yield with a single transformation step, check the box below the drawing area. Note for advanced students: you may assume that an excess of benzene is used as part of the reaction conditions. : ☐ + I X This product can't be made in a single transformation step.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning


