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Contents

   



(Top)
 


1 Trans isomer  



1.1  Preparation  





1.2  Hydrates  





1.3  Reactions  







2 Cis isomer  



2.1  Preparation  





2.2  Properties and reactions  







3 See also  





4 References  














Sodium hyponitrite






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Sodium hyponitrite (trans isomer)
Identifiers

CAS Number

3D model (JSmol)

  • trans-form: Interactive image
  • cis-form: Interactive image
  • ChemSpider

    PubChem CID

    CompTox Dashboard (EPA)

    • InChI=1S/H2N2O2.2Na/c3-1-2-4;;/h(H,1,4)(H,2,3);;/q;2*+1/p-2

      Key: HLJWMCUZPYEUDI-UHFFFAOYSA-L

    • N(=N[O-])[O-].[Na+].[Na+]

    • trans-form: [Na+].[O-]/N=N/[O-].[Na+]

    • cis-form: [Na+].[O-]\N=N/[O-].[Na+]

    Properties

    Chemical formula

    Na2N2O2
    Molar mass 105.99 g/mol
    Appearance colorless crystals
    Density 2.466 g/cm3
    Melting point 100 °C (212 °F; 373 K)
    Boiling point 335 °C (635 °F; 608 K) decomposes

    Solubility in water

    soluble
    Solubility insoluble in ethanol

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    Infobox references

    Sodium hyponitrite is a solid ionic compound with formula Na
    2
    N
    2
    O
    2
    or (Na+
    )2[ON=NO]2−.[1]

    There are cis and trans forms of the hyponitrite ion N
    2
    O2−
    2
    . The trans form is more common, but the cis form can be obtained too, and it is more reactive than the trans form.[1][2]

    Trans isomer[edit]

    The trans isomer is colorless and soluble in water and insoluble in ethanol and ether.[3][4]

    Preparation[edit]

    Sodium hyponitrite (trans) is conventionally prepared by reductionofsodium nitrite with sodium amalgam.[5][6][7]

    2 NaNO2 + 4 Na(Hg) + 2 H2O → Na2N2O2 + 4 NaOH + 4 Hg

    Sodium hyponitrite (trans) was prepared in 1927 by A. W. Scott by reacting alkyl nitrites, hydroxylammonium chloride, and sodium ethoxide[4][8]

    RONO + NH2OH + 2 EtONa → Na2N2O2 + ROH + 2 EtOH

    An earlier method, published by D. Mendenhall in 1974, reacted gaseous nitric oxide (NO) with sodium metal in 1,2-dimethoxyethane, toluene, and benzophenone. The salt was then extracted with water.[9] The method was later modified to use pyridine[citation needed].

    Other methods included oxidation of a concentrated solution of hydroxylamine with sodium nitrite in an alkaline medium[citation needed]; or electrolysis of sodium nitrite.[10]

    Hydrates[edit]

    A variety of hydrates Na
    2
    N
    2
    O
    2
    (H
    2
    O
    )x of the trans isomer have been reported, with x including 2, 3.5, 4, 5, 6, 7, 8, and 9;[11][3][12] but there is some dispute.[13]

    The hydration water seems to be just trapped in the crystal lattice rather than coordinated to the ions.[13] The anhydrous substance can be obtained by drying the hydrates over phosphorus pentoxide and then heating them to 120 °C.[13]

    Reactions[edit]

    Sodium hyponitrite (trans) in solution is decomposed by carbon dioxide CO
    2
    from air to form sodium carbonate.[14]

    Liquid N2O4 oxidises sodium hyponitrite (trans) to give sodium peroxohyponitrite Na2+
    2
    [ON=NOO]2−).[15][1]

    Cis isomer[edit]

    The cis isomer of sodium hyponitrite is a white crystalline solid, insoluble in aprotic solvents, and (unlike the trans isomer) decomposed by water and other protic solvents.[2]

    Preparation[edit]

    The cis isomer of can be prepared by passing nitric oxide (NO) through a solution of sodium metal in liquid ammonia at −50 °C.[1]

    The cis isomer was also obtained in 1996 by C. Feldmann and M. Jansen by heating sodium oxide Na
    2
    O
    with 77 kPaofnitrous oxide N
    2
    O
    (laughing gas) in a sealed tube at 360 °C for 2 hours. The two reagents combined to yield the cis hyponitrite quantitatively as white microcrystals.[8][2]

    Properties and reactions[edit]

    The anhydrous cis salt is stable up to 325 °C, when it disproportionates to nitrogen and sodium orthonitrite:[2]

    3Na
    2
    N
    2
    O
    2
    → 2 Na
    3
    O
    (NO
    2
    ) + 2 N
    2

    It is generally more reactive than the trans isomer.[1]

    See also[edit]

    References[edit]

    1. ^ a b c d e Egon Wiberg, Arnold Frederick Holleman (2001) Inorganic Chemistry, Elsevier ISBN 0-12-352651-5
  • ^ a b c d Claus Feldmann, Martin Jansen (1996), "cis-Sodium Hyponitrite - A New Preparative Route and a Crystal Structure Analysis". Angewandte Chemie International Edition in English, volume 35, issue 15, pages 1728–1730. doi:10.1002/anie.199617281
  • ^ a b Trambaklal Mohanlal Oza, Rajnikant Hariprasad Thaker (1955), "The Thermal Decomposition of Silver Hyponitrite". Journal of the American Chemical society, volume 77, issue 19, pages 4976–4980. doi:10.1021/ja01624a007
  • ^ a b A. W. Scott (1927), "Sodium Hyponitrite". J. Am. Chem. Soc., volume = 49, issue 4, pages = 986–987. doi:10.1021/ja01403a502
  • ^ Addison, C. C.; Gamlen G. A.; Thompson, R. (1952). "70. The ultra-violet absorption spectra of sodium hyponitrite and sodium α-oxyhyponitrite : the analysis of mixtures with sodium nitrite and nitrate". J. Chem. Soc.: 338–345. doi:10.1039/jr9520000338.
  • ^ Neumann, R. C., Jr. Bussey, R. J. (1970). "High pressure studies. V. Activation volumes for combination and diffusion of geminate tert-butoxy radicals". J. Am. Chem. Soc. 92 (8): 2440–2445. doi:10.1021/ja00711a039.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  • ^ a b Catherine E. Housecroft; Alan G. Sharpe (2008). "Chapter 15: The group 15 elements". Inorganic Chemistry (3rd ed.). Pearson. p. 468. ISBN 978-0-13-175553-6.
  • ^ G. David Mendenhall (1974), "Convenient synthesis of silver hyponitrite". Journal of the American Chemical society, volume 96, issue 15, page 5000. doi:10.1021/ja00822a054
  • ^ Polydoropoulos, C. N. Chem. Ind. (London) 1963, 1686 and references therein.
  • ^ James Riddick Partington and Chandulal Chhotalal Shah (1931), "Investigations on hyponitrites. Part I. Sodium hyponitrite: preparation and properties". Journal of the Chemical Society (Resumed), paper CCLXXXII, pages 2071-2080. doi:10.1039/JR9310002071
  • ^ C.N. Polydoropoulos, S.D. Voliotis (1967), "Sodium hyponitrite hexahydrate". Journal of Inorganic and Nuclear Chemistry, volume 29, issue 12, pages 2899–2901. doi:10.1016/0022-1902(67)80121-0
  • ^ a b c Gary L. Stucky, Jack L. Lambert, R. Dean Dragsdorf (1969), "The hydrates of sodium hyponitrite". Journal of Inorganic and Nuclear Chemistry, volume 31, issue 1, pages 29–32 doi:10.1016/0022-1902(69)80050-3
  • ^ Charlotte N. Conner, Caroline E. Donald, Martin N. Hughes, Christina Sami (1989), "The molar absorptivity of sodium hyponitrite". Polyhedron, volume 8, issue 21, pages 2621-2622. doi:10.1016/S0277-5387(00)81166-3
  • ^ M. N. Hughes and H. G. Nicklin (1969), "The action of dinitrogen tetroxide on sodium hyponitrite". Journal of the Chemical Society D: Chemical Communications, volume 1969, issue 2, page 80a. doi:10.1039/C2969000080A

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