
Concept explainers
(a)
Interpretation:
Which underlined proton has the greater chemical shift has to be determined.
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.
(b)
Interpretation:
Which underlined proton has the greater chemical shift has to be determined.
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.
(c)
Interpretation:
Which underlined proton has the greater chemical shift has to be determined.
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.
(d)
Interpretation:
Which underlined proton has the greater chemical shift has to be determined.
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.
(e)
Interpretation:
Which underlined proton has the greater chemical shift has to be determined.
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.
(f)
Interpretation:
Which underlined proton has the greater chemical shift has to be determined.
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.

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Chapter 14 Solutions
Organic Chemistry (8th Edition)
- Organic Functional Groups Predicting the reactants or products of acetal hydrolysis termine the structures of the missing organic molecules in the following reaction: H* H* + H₂O Y ☑ Note: Molecules that share the same letter have the exact same structure. In the drawing area below, draw the skeletal ("line") structures of the missing organic molecules X, Y, and Z. You may draw that you like, so long as they aren't touching. Molecule X shows up in multiple steps, but you only have to draw its structure Explanation Check @2 W Click and drag to start drawing a structure. #4 # 3 LU E % 67 olo 5 66 R T Y & 7 AcGraw Hill LLC. All Rights R Xarrow_forward8. (16 pts) Provide the stepwise mechanism for the synthesis of the following compound via an enaminearrow_forwardDraw the titration curve of (i) weak acid vs. strong base; (ii) weak acid vs. weakbase; (iii) diprotic acid with strong base (iii) triprotic acid with strong base.arrow_forward
- Complete the reaction in the drawing area below by adding the major products to the right-hand side. If there won't be any products, because nothing will happen under these reaction conditions, check the box under the drawing area instead. Note: if the products contain one or more pairs of enantiomers, don't worry about drawing each enantiomer with dash and wedge bonds. Just draw one molecule to represent each pair of enantiomers, using line bonds at the chiral center. More... No reaction. my ㄖˋ + 1. Na O Me Click and drag to start drawing a structure. 2. H +arrow_forwardPredict the intermediate 1 and final product 2 of this organic reaction: NaOMe H+ + 1 2 H H work up You can draw 1 and 2 in any arrangement you like. Note: if either 1 or 2 consists of a pair of enantiomers, just draw one structure using line bonds instead of 3D (dash and wedge) bonds at the chiral center. Click and drag to start drawing a structure. X $ dmarrow_forwardPredict the major products of this organic reaction: 1. NaH (20°C) 2. CH3Br ? Some notes: • Draw only the major product, or products. You can draw them in any arrangement you like. • Be sure to use wedge and dash bonds where necessary, for example to distinguish between major products that are enantiomers. • If there are no products, just check the box under the drawing area. No reaction. Click and drag to start drawing a structure. G Crarrow_forward
- Predict the major products of this organic reaction: 1. LDA (-78°C) ? 2. Br Some notes: • Draw only the major product, or products. You can draw them in any arrangement you like. . • Be sure to use wedge and dash bonds where necessary, for example to distinguish between major products that are enantiomers. • If there are no products, just check the box under the drawing area. No reaction. Click and drag to start drawing a structure. Xarrow_forwardPlease draw the structuresarrow_forwardDraw the missing intermediates 1 and 2, plus the final product 3, of this synthesis: 0 1. Eto 1. Eto- 1 2 2. MeBr 2. EtBr H3O+ A 3 You can draw the three structures in any arrangement you like. Explanation Check Click and drag to start drawing a structure.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning

