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EBK ORGANIC CHEMISTRY
6th Edition
ISBN: 8220103151757
Author: LOUDON
Publisher: MAC HIGHER
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Question
Chapter 4, Problem 4.38P
Interpretation Introduction
Interpretation:
An explanation as to why the hydration reaction of ethylene is a very slow reaction is to be stated.
Concept introduction:
Hammond’s postulate states that the structure and energy of the transition state of a reaction depends on free energy of transition state. A reaction having intermediate with relatively higher free energy than the reactant and products can be approximated using the structure and energy of intermediate.
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Students have asked these similar questions
1. (a) Describe aromaticity, Kekule structure and resonance structure for benzene.
(b) Why is benzene more stable than aliphatic alkenes?
Answer ALL parts of this question.
(a) Using resonance structures, discuss the following statement; phenols are much
stronger acids than aliphatic alcohols.
(b) Give the structure of a stronger organic acid than phenol.
(c) Rationalise the acidity of the latter organic acid by drawing two resonance
structures of the conjugate base.
(d) Eugenol is a natural product derived from the dried flower buds of the evergreen
tree, Eugenia aromatica. Briefly describe a procedure with reagents required to
extract eugenol as a single component from the mixture of compounds present in
these flower buds.
OH
LOCH 3
eugenol
Can the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating
the reactants?
?
A
Chapter 4 Solutions
EBK ORGANIC CHEMISTRY
Ch. 4 - Prob. 4.1PCh. 4 - Prob. 4.2PCh. 4 - Prob. 4.3PCh. 4 - Prob. 4.4PCh. 4 - Prob. 4.5PCh. 4 - Prob. 4.6PCh. 4 - Prob. 4.7PCh. 4 - Prob. 4.8PCh. 4 - Prob. 4.9PCh. 4 - Prob. 4.10P
Ch. 4 - Prob. 4.11PCh. 4 - Prob. 4.12PCh. 4 - Prob. 4.13PCh. 4 - Prob. 4.14PCh. 4 - Prob. 4.15PCh. 4 - Prob. 4.16PCh. 4 - Prob. 4.17PCh. 4 - Prob. 4.18PCh. 4 - Prob. 4.19PCh. 4 - Prob. 4.20PCh. 4 - Prob. 4.21PCh. 4 - Prob. 4.22PCh. 4 - Prob. 4.23PCh. 4 - Prob. 4.24PCh. 4 - Prob. 4.25PCh. 4 - Prob. 4.26PCh. 4 - Prob. 4.27PCh. 4 - Prob. 4.28PCh. 4 - Prob. 4.29PCh. 4 - Prob. 4.30PCh. 4 - Prob. 4.31PCh. 4 - Prob. 4.32PCh. 4 - Prob. 4.33PCh. 4 - Prob. 4.34PCh. 4 - Prob. 4.35PCh. 4 - Prob. 4.36PCh. 4 - Prob. 4.37PCh. 4 - Prob. 4.38PCh. 4 - Prob. 4.39PCh. 4 - Prob. 4.40APCh. 4 - Prob. 4.41APCh. 4 - Prob. 4.42APCh. 4 - Prob. 4.43APCh. 4 - Prob. 4.44APCh. 4 - Prob. 4.45APCh. 4 - Prob. 4.46APCh. 4 - Prob. 4.47APCh. 4 - Prob. 4.48APCh. 4 - Prob. 4.49APCh. 4 - Prob. 4.50APCh. 4 - Prob. 4.51APCh. 4 - Prob. 4.52APCh. 4 - Prob. 4.53APCh. 4 - Prob. 4.54APCh. 4 - Prob. 4.55APCh. 4 - Prob. 4.56APCh. 4 - Prob. 4.57APCh. 4 - Prob. 4.58APCh. 4 - Prob. 4.59APCh. 4 - Prob. 4.60APCh. 4 - Prob. 4.61APCh. 4 - Prob. 4.62APCh. 4 - Prob. 4.63APCh. 4 - Prob. 4.64APCh. 4 - Prob. 4.65APCh. 4 - Prob. 4.66APCh. 4 - Prob. 4.67APCh. 4 - Prob. 4.68APCh. 4 - Prob. 4.69APCh. 4 - Prob. 4.70AP
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- 2. a) Draw the structures of Perylene dianhydride, Naphthalene and Salicylic acid b) Arrange the compounds in order of increasing polarity considering the structures and Rf valuesarrow_forwardDraw the structures of the following compounds. (a) isobutyl bromidearrow_forwardWhich of the following is true for the reactions of alkyl halides? (a) The characteristic reactions of alkyl halides are oxidation and reduction.(b) The characteristic reactions of alkyl halides are elimination and substitutionc. The characteristic reactions of alkyl halides are addition and substitutiond. Characteristic reactions of alkyl halides are addition and elimination.arrow_forward
- Although benzene is normally written with three double bonds, benzene is not reactive towards many reagents that alkenes normally react with. This lack of reactivity can be explained by the unusual stability created by cyclic conjugation. First, (i) describe at least one of the physical properties of benzene that demonstrates how the true structure of benzene does match the way the structure is normally written. Then, (ii) explain how the unusual stability of benzene can be demonstrated by its thermodynamic properties through some form of experiment. Be sure to (iii) include an appropriately labeled diagram as part of your answer (you do not have to quote any numerical values).arrow_forward6. Describe concisely a chemical test to distinguish between the following pairs of compounds. (a) n-pentanol and 3-methylpentan-3-ol (b) Ethanal dan pentanal (c) Phenol and benzoic acidarrow_forwardWhat will be the color of the flame and the amount of soot if the following are ignited:(a) Hexane (b)Heptane(c) Cyclohexane (d) Cyclohexene (e) Benzene (f) Toluenearrow_forward
- (a) One test for the presence of an alkene is to add a smallamount of bromine, which is a red-brown liquid, and lookfor the disappearance of the red-brown color. This test doesnot work for detecting the presence of an aromatic hydrocarbon.Explain. (b) Write a series of reactions leading topara-bromoethylbenzene, beginning with benzene andusing other reagents as needed. What isomeric side productsmight also be formed?arrow_forwardHydrocarbon A possesses a significant dipole, even though it iscomposed of only C—C and C—H bonds. Explain why the dipole arisesand use resonance structures to illustrate the direction of the dipole.Which ring is more electron rich?arrow_forward1. (a) Indene is considered much acidic compare to most hydrocarbons. It is readily reacting with strong base such as NaNH2 to form its conjugate base. + NANH2 + NH3 Nat indene (i) Draw the conjugate base of indene. (ii) Explain why indene is much acidic compare to most hydrocarbons.arrow_forward
- 6. Briefly outline an experiment that would allow you to distinguish between alkanes, carboxylic acids and ketones based on their physical properties. explain your rationale. 1arrow_forward6. Describe concisely a chemical test to distinguish between the following pairs of compounds. Terangkan secara ringkas ujian kimia bagi membezakan pasangan sebatian berikut. (a) Propanal and propanone (b) Phenol and benzoic acid (c) Hexan-3-one and hexan-2-onearrow_forwardb) Which of these two would you expect to have the higher boiling point? Why? hexanal c) Write "most" under Write "least" under benzonitrile pentanoic acid compound which will react with Cly/FeCl, most easily. compound which will be least reactive toward Cly/FeCl. ethylbenzene chlorobenzenearrow_forward
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