(a)
Interpretation:
Structural formula of the parent acid and parent alcohol for the given ester molecule has to be drawn.
Concept Introduction:
Esters are prepared by condensation of
Esterification reaction is the one in which the carboxylic acid is condensed with an alcohol (or phenol) in presence of strong acid catalyst to produce ester. The general reaction scheme can be given as,
In the above reaction, hydroxyl group is lost from carboxylic acid and hydrogen is lost from alcohol molecule to form water as the byproduct.
(b)
Interpretation:
Structural formula of the parent acid and parent alcohol for the given ester molecule has to be drawn.
Concept Introduction:
Esters are prepared by condensation of carboxylic acid with an alcohol. A molecule of water is lost on this reaction. The reaction that takes place in producing esters is known as esterification reaction.
Esterification reaction is the one in which the carboxylic acid is condensed with an alcohol (or phenol) in presence of strong acid catalyst to produce ester. The general reaction scheme can be given as,
In the above reaction, hydroxyl group is lost from carboxylic acid and hydrogen is lost from alcohol molecule to form water as the byproduct.
(c)
Interpretation:
Structural formula of the parent acid and parent alcohol for the given ester molecule has to be drawn.
Concept Introduction:
Esters are prepared by condensation of carboxylic acid with an alcohol. A molecule of water is lost on this reaction. The reaction that takes place in producing esters is known as esterification reaction.
Esterification reaction is the one in which the carboxylic acid is condensed with an alcohol (or phenol) in presence of strong acid catalyst to produce ester. The general reaction scheme can be given as,
In the above reaction, hydroxyl group is lost from carboxylic acid and hydrogen is lost from alcohol molecule to form water as the byproduct.
(d)
Interpretation:
Structural formula of the parent acid and parent alcohol for the given ester molecule has to be drawn.
Concept Introduction:
Esters are prepared by condensation of carboxylic acid with an alcohol. A molecule of water is lost on this reaction. The reaction that takes place in producing esters is known as esterification reaction.
Esterification reaction is the one in which the carboxylic acid is condensed with an alcohol (or phenol) in presence of strong acid catalyst to produce ester. The general reaction scheme can be given as,
In the above reaction, hydroxyl group is lost from carboxylic acid and hydrogen is lost from alcohol molecule to form water as the byproduct.
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Chapter 16 Solutions
General, Organic, and Biological Chemistry Seventh Edition
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- Don't used hand raitingarrow_forwardDon't used hand raitingarrow_forwardRelative Intensity Part VI. consider the multi-step reaction below for compounds A, B, and C. These compounds were subjected to mass spectrometric analysis and the following spectra for A, B, and C was obtained. Draw the structure of B and C and match all three compounds to the correct spectra. Relative Intensity Relative Intensity 100 HS-NJ-0547 80 60 31 20 S1 84 M+ absent 10 30 40 50 60 70 80 90 100 100- MS2016-05353CM 80- 60 40 20 135 137 S2 164 166 0-m 25 50 75 100 125 150 m/z 60 100 MS-NJ-09-43 40 20 20 80 45 S3 25 50 75 100 125 150 175 m/zarrow_forward
- Don't used hand raiting and don't used Ai solutionarrow_forwardPredicting the pro Predict the major products of this organic reaction. Explanation Check m ☐ + 5 1.03 Click and drag t drawing a stru 2. (CH₂)₂S 3 2 © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forwardstarting 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... X Explanation Check C टे Br T Add/Remove step ☐ Br Br © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacarrow_forward
- Don't used hand raitingarrow_forwardRelative Intensity Part VI. consider the multi-step reaction below for compounds A, B, and C. These compounds were subjected to mass spectrometric analysis and the following spectra for A, B, and C was obtained. Draw the structure of B and C and match all three compounds to the correct spectra. Relative Intensity Relative Intensity 100 HS-NJ-0547 80 60 31 20 S1 84 M+ absent 10 30 40 50 60 70 80 90 100 100- MS2016-05353CM 80- 60 40 20 135 137 S2 164 166 0-m 25 50 75 100 125 150 m/z 60 100 MS-NJ-09-43 40 20 20 80 45 S3 25 50 75 100 125 150 175 m/zarrow_forwardPart II. Given two isomers: 2-methylpentane (A) and 2,2-dimethyl butane (B) answer the following: (a) match structures of isomers given their mass spectra below (spectra A and spectra B) (b) Draw the fragments given the following prominent peaks from each spectrum: Spectra A m/2 =43 and 1/2-57 spectra B m/2 = 43 (c) why is 1/2=57 peak in spectrum A more intense compared to the same peak in spectrum B. Relative abundance Relative abundance 100 A 50 29 29 0 10 -0 -0 100 B 50 720 30 41 43 57 71 4-0 40 50 60 70 m/z 43 57 8-0 m/z = 86 M 90 100 71 m/z = 86 M -O 0 10 20 30 40 50 60 70 80 -88 m/z 90 100arrow_forward
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