Cyclopropanecarboxaldehyde


Gas phase ion energetics data

Go To: Top, Mass spectrum (electron ionization), Gas Chromatography, References, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: John E. Bartmess

View reactions leading to C4H6O+ (ion structure unspecified)

De-protonation reactions

C4H5O- + Hydrogen cation = Cyclopropanecarboxaldehyde

By formula: C4H5O- + H+ = C4H6O

Quantity Value Units Method Reference Comment
Δr1631. ± 21.kJ/molG+TSBaschky, Peterson, et al., 1994gas phase; Between D2O and PhF. Cis and Trans anions do not interconvert and have same expt. acidity.
Quantity Value Units Method Reference Comment
Δr1598. ± 21.kJ/molIMRBBaschky, Peterson, et al., 1994gas phase; Between D2O and PhF. Cis and Trans anions do not interconvert and have same expt. acidity.

C4H5O- + Hydrogen cation = Cyclopropanecarboxaldehyde

By formula: C4H5O- + H+ = C4H6O

Quantity Value Units Method Reference Comment
Δr1572. ± 8.8kJ/molG+TSChou, Dahlke, et al., 1993gas phase; barrier for opening to CH2=C(CHO)CH2-: 29 kcal/mol.
Quantity Value Units Method Reference Comment
Δr1543. ± 8.4kJ/molIMREChou, Dahlke, et al., 1993gas phase; barrier for opening to CH2=C(CHO)CH2-: 29 kcal/mol.

Mass spectrum (electron ionization)

Go To: Top, Gas phase ion energetics data, Gas Chromatography, References, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

Notice: This spectrum may be better viewed with a Javascript and HTML 5 enabled browser.

Mass spectrum
For Zoom
1.) Enter the desired X axis range (e.g., 100, 200)
2.) Check here for automatic Y scaling
3.) Press here to zoom

Additional Data

View image of digitized spectrum (can be printed in landscape orientation).

Due to licensing restrictions, this spectrum cannot be downloaded.

Owner NIST Mass Spectrometry Data Center
Collection (C) 2014 copyright by the U.S. Secretary of Commerce
on behalf of the United States of America. All rights reserved.
Origin Chemical Concepts
NIST MS number 162751

All mass spectra in this site (plus many more) are available from the NIST/EPA/NIH Mass Spectral Library. Please see the following for information about the library and its accompanying search program.


Gas Chromatography

Go To: Top, Gas phase ion energetics data, Mass spectrum (electron ionization), References, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Normal alkane RI, non-polar column, custom temperature program

View large format table.

Column type Active phase I Reference Comment
CapillaryMethyl Silicone617.Zenkevich, 1996Program: not specified

References

Go To: Top, Gas phase ion energetics data, Mass spectrum (electron ionization), Gas Chromatography, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Baschky, Peterson, et al., 1994
Baschky, M.C.; Peterson, K.C.; Kass, S.R., Stereospecificity in the gas phase. Formation and characterization of configurationally stable cyclopropyl anions, J. Am. Chem. Soc., 1994, 116, 16, 7218, https://doi.org/10.1021/ja00095a026 . [all data]

Chou, Dahlke, et al., 1993
Chou, P.K.; Dahlke, G.D.; Kass, S.R., Unimolecular Rearrangements of Carbanions in the Gas Phase .2. Cyclopropyl Anions, J. Chem. Soc. Chem. Comm., 1993, 115, 1, 315, https://doi.org/10.1021/ja00054a045 . [all data]

Zenkevich, 1996
Zenkevich, I.G., Informational Maitenance of Gas Chromatographic Identification of Organic Compounds in Ecoanalytical Investigations, Z. Anal. Chem., 1996, 51, 11, 1140-1148. [all data]


Notes

Go To: Top, Gas phase ion energetics data, Mass spectrum (electron ionization), Gas Chromatography, References