Propanol to propane: An advanced laboratory experiment using heterogeneous catalysts for two successive gas-phase reactions

Bruce Mattson; Martin Hulce; Wes Cheng; Jaclyn Greimann; Trisha Hoette; Peter Menzel

doi:10.1021/ed083p421

Propanol to propane: An advanced laboratory experiment using heterogeneous catalysts for two successive gas-phase reactions

Bruce Mattson, Martin Hulce, Wes Cheng, Jaclyn Greimann, Trisha Hoette, Peter Menzel

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

8 Scopus citations

Abstract

A sequence of two organic reactions involving gas-phase heterogeneous catalysis suitable for use as a laboratory experiment is outlined. In the first reaction, 2-propanol is converted to propene using alumina beads as the catalyst. The product gas is purified with a mini-cold trap. In the second reaction, propene is hydrogenated to propane using a palladium catalyst in nearly 100% yield. The experiment demonstrates continuous-flow, closed-system gas-phase reactions of fundamental importance in chemical industry. It also demonstrates the power of NMR in the context for which it actually is used by organic and inorganic chemists: structural confirmation and analysis.

Original language	English (US)
Pages (from-to)	421-424
Number of pages	4
Journal	Journal of chemical education
Volume	83
Issue number	3
DOIs	https://doi.org/10.1021/ed083p421
State	Published - Mar 2006

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Chemistry(all)
Education

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title = "Propanol to propane: An advanced laboratory experiment using heterogeneous catalysts for two successive gas-phase reactions",

abstract = "A sequence of two organic reactions involving gas-phase heterogeneous catalysis suitable for use as a laboratory experiment is outlined. In the first reaction, 2-propanol is converted to propene using alumina beads as the catalyst. The product gas is purified with a mini-cold trap. In the second reaction, propene is hydrogenated to propane using a palladium catalyst in nearly 100% yield. The experiment demonstrates continuous-flow, closed-system gas-phase reactions of fundamental importance in chemical industry. It also demonstrates the power of NMR in the context for which it actually is used by organic and inorganic chemists: structural confirmation and analysis.",

author = "Bruce Mattson and Martin Hulce and Wes Cheng and Jaclyn Greimann and Trisha Hoette and Peter Menzel",

year = "2006",

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doi = "10.1021/ed083p421",

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AU - Mattson, Bruce

AU - Hulce, Martin

AU - Cheng, Wes

AU - Greimann, Jaclyn

AU - Hoette, Trisha

AU - Menzel, Peter

PY - 2006/3

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N2 - A sequence of two organic reactions involving gas-phase heterogeneous catalysis suitable for use as a laboratory experiment is outlined. In the first reaction, 2-propanol is converted to propene using alumina beads as the catalyst. The product gas is purified with a mini-cold trap. In the second reaction, propene is hydrogenated to propane using a palladium catalyst in nearly 100% yield. The experiment demonstrates continuous-flow, closed-system gas-phase reactions of fundamental importance in chemical industry. It also demonstrates the power of NMR in the context for which it actually is used by organic and inorganic chemists: structural confirmation and analysis.

AB - A sequence of two organic reactions involving gas-phase heterogeneous catalysis suitable for use as a laboratory experiment is outlined. In the first reaction, 2-propanol is converted to propene using alumina beads as the catalyst. The product gas is purified with a mini-cold trap. In the second reaction, propene is hydrogenated to propane using a palladium catalyst in nearly 100% yield. The experiment demonstrates continuous-flow, closed-system gas-phase reactions of fundamental importance in chemical industry. It also demonstrates the power of NMR in the context for which it actually is used by organic and inorganic chemists: structural confirmation and analysis.

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JF - Journal of Chemical Education

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Propanol to propane: An advanced laboratory experiment using heterogeneous catalysts for two successive gas-phase reactions

Abstract

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