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Related Concept Videos

Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration02:34

Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration

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The rate of acid-catalyzed hydration of alkenes depends on the alkene's structure, as the presence of alkyl substituents at the double bond can significantly influence the rate.
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Aldehydes and Ketones with Water: Hydrate Formation01:20

Aldehydes and Ketones with Water: Hydrate Formation

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An oxygen-based nucleophile, like water, can undergo addition reactions with aldehydes and ketones. The reaction leads to the formation of hydrates, also referred to as 1,1-diols or geminal diols.
The formation of hydrates is a reversible reaction. Hydrate formation is influenced by steric and electronic factors accompanying the alkyl substituents on the carbonyl group: The rate of hydrate formation increases with a decrease in the number of alkyl groups attached to the carbonyl carbon. Hence,...
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Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration02:40

Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration

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Introduction
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.
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Formation of Halohydrin from Alkenes02:41

Formation of Halohydrin from Alkenes

15.0K
An alkene, such as propene, reacts with bromine in the presence of water to yield a halohydrin. Halohydrins contain a halogen and a hydroxyl group attached to adjacent carbons. When the halogen is bromine, it is called a bromohydrin, while a chlorohydrin has chlorine as the halogen.
15.0K
Acid-Catalyzed Hydration of Alkenes02:45

Acid-Catalyzed Hydration of Alkenes

18.2K
Alkenes react with water in the presence of an acid to form an alcohol. In the absence of acid, hydration of alkenes does not occur at a significant rate, and the acid is not consumed in the reaction. Therefore, alkene hydration is an acid-catalyzed reaction.
18.2K
Multiple Halogenation of Methyl Ketones: Haloform Reaction01:28

Multiple Halogenation of Methyl Ketones: Haloform Reaction

3.1K
A method involving the transformation of methyl ketones to carboxylic acids using excess base and halogen is called the haloform reaction. It begins with the deprotonation of α hydrogen to form an enolate ion which reacts with the electrophilic halogen to give an α-halo ketone. The step continues until all the α protons are substituted to form a trihalomethyl ketone. The resulting molecule is unstable, and in the presence of a hydroxide base, it readily undergoes nucleophilic...
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Methane Hydrate Crystallization on Sessile Water Droplets
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Propane Clathrate Hydrate Formation Accelerated by Methanol.

Jaruwan Amtawong1, Jin Guo1, Jared S Hale1

  • 1Department of Chemistry, University of California , Irvine, California 92697, United States.

The Journal of Physical Chemistry Letters
|June 9, 2016
PubMed
Summary

Methanol significantly accelerates propane clathrate hydrate (CH) formation even at low concentrations. This discovery aids efficient gas storage and provides insights into CH formation mechanisms.

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Area of Science:

  • Physical Chemistry
  • Materials Science

Background:

  • Methanol's dual role as inhibitor and catalyst in clathrate hydrate (CH) formation is under investigation.
  • Understanding CH kinetics is crucial for applications like gas storage.

Purpose of the Study:

  • To quantitatively study the kinetics of propane CH formation at 253 K.
  • To investigate the effect of methanol doping on CH formation rates and initiation pressure.

Main Methods:

  • Propane gas reacted with <75 μm ice particles doped with varying methanol concentrations at 253 K.
  • Quantitative kinetic measurements of propane uptake into CHs.

Main Results:

  • Methanol significantly accelerates propane CH formation kinetics, even at low doping levels (1 methanol per 10,000 water molecules).
  • Enhanced uptake rates and reduced initiation pressure observed with methanol doping.
  • The acceleration effect is pronounced even with minimal methanol presence.

Conclusions:

  • Small quantities of methanol act as potent catalysts for propane clathrate hydrate formation.
  • Findings suggest potential for more efficient CH production for gas storage applications.
  • The observed acceleration may refine mechanistic understanding of methanol's role in CH formation under different conditions.