Carbonic acid

Carbonic acid
Names
	Preferred IUPAC name Carbonic acid[1]
	Other names Carbon dioxide solution; Dihydrogen carbonate; Hydrogen bicarbonate; Acid of air; Aerial acid; Hydroxymethanoic acid
Identifiers
CAS Number	463-79-6 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:28976 ;
ChEMBL	ChEMBL1161632 ;
ChemSpider	747 ;
ECHA InfoCard	100.133.015
EC Number	610-295-3
KEGG	C01353 ;
PubChem CID	767;
	InChI InChI=1S/CH2O3/c2-1(3)4/h(H2,2,3,4) Key: BVKZGUZCCUSVTD-UHFFFAOYSA-N ; InChI=1/CH2O3/c2-1(3)4/h(H2,2,3,4) Key: BVKZGUZCCUSVTD-UHFFFAOYAU;
	SMILES O=C(O)O;
Properties
Chemical formula	H2CO3
Molar mass	62.03 g/mol
Density	1.668 g/cm3
Solubility in water	Only stable in solution
Acidity (pKa)	3.6 (pKa1 for H2CO3 only), 6.3 (pKa1 including CO2(aq)), 10.32 (pKa2)
Conjugate base	Bicarbonate
Related compounds
Related compounds	Acetone ; Urea ; Carbonyl fluoride
Hazards
NFPA 704	0 0 1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

Not to be confused with Carbolic acid, an antiquated name for phenol.

Carbonic acid is a chemical compound with the chemical formula H₂CO₃ (equivalently OC(OH)₂). It is also a name sometimes given to solutions of carbon dioxide in water (carbonated water), because such solutions contain small amounts of H₂CO₃. In physiology, carbonic acid is described as volatile acid or respiratory acid, because it is the only acid excreted as a gas by the lungs.^[2] It plays an important role in the bicarbonate buffer system to maintain acid–base homeostasis.

Carbonic acid, which is a weak acid, forms two kinds of salts: the carbonates and the bicarbonates. In geology, carbonic acid causes limestone to dissolve, producing calcium bicarbonate, which leads to many limestone features such as stalactites and stalagmites.

It was long believed that carbonic acid could not exist as a pure compound. However, in 1991 it was reported that NASA scientists had succeeded in making solid H₂CO₃ samples.^[3]

Chemical equilibrium

When carbon dioxide dissolves in water it exists in chemical equilibrium with carbonic acid:^[4]

{\ce {CO2 + H2O <=> H2CO3}}

The hydration equilibrium constant at 25 °C is called K_h, which in the case of carbonic acid is [H₂CO₃]/[CO₂] ≈ 1.7×10⁻³ in pure water^[5] and ≈ 1.2×10⁻³ in seawater.^[6] Hence, the majority of the carbon dioxide is not converted into carbonic acid, remaining as CO₂ molecules. In the absence of a catalyst, the equilibrium is reached quite slowly. The rate constants are 0.039 s⁻¹ for the forward reaction (CO₂ + H₂O → H₂CO₃) and 23 s⁻¹ for the reverse reaction (H₂CO₃ → CO₂ + H₂O). The addition of two molecules of water to CO₂ would give orthocarbonic acid, C(OH)₄, which exists only in minute amounts in aqueous solution.

Addition of base to an excess of carbonic acid gives bicarbonate (hydrogen carbonate). With excess base, carbonic acid reacts to give carbonate salts.

Role of carbonic acid in blood

Bicarbonate is an intermediate in the transport of CO₂ out of the body by respiratory gas exchange. The hydration reaction of CO₂ is generally very slow in the absence of a catalyst, but red blood cells contain carbonic anhydrase, which increases the reaction rate, producing bicarbonate (HCO₃⁻) dissolved in the blood plasma. This catalysed reaction is reversed in the lungs, where it converts the bicarbonate back into CO₂ and allows it to be expelled. This equilibration plays an important role as a buffer in mammalian blood.^[7] A 2016 theoretical report suggests that carbonic acid may play a pivotal role in protonating various nitrogen bases in blood serum.^[8]

Role of carbonic acid in ocean chemistry

The oceans of the world have absorbed almost half of the CO₂ emitted by humans from the burning of fossil fuels.^[9] It has been estimated that the extra dissolved carbon dioxide has caused the ocean's average surface pH to shift by about −0.1 unit from pre-industrial levels. This is known as ocean acidification, even though the ocean remains basic.^[10]

Acidity of carbonic acid

Carbonic acid is a carboxylic acid with a hydroxyl group as the substituent. It is also a polyprotic acid — specifically it is diprotic, meaning that it has two protons that may dissociate from the parent molecule. Thus, there are two dissociation constants, first of which is for the dissociation into the bicarbonate (also called hydrogen carbonate) ion HCO₃⁻:

{\ce {H2CO3 <=> HCO3^- + H+}}

K_a1 = 2.5×10⁻⁴;^[4] pK_a1 = 3.6 at 25 °C.

Care must be taken when quoting and using the first dissociation constant of carbonic acid. In aqueous solution, carbonic acid exists in equilibrium with carbon dioxide, and the concentration of H₂CO₃ is much lower than the concentration of CO₂. In many analyses, H₂CO₃ includes dissolved CO₂ (referred to as CO₂(aq)), H₂CO₃* is used to represent the two species when writing the aqueous chemical equilibrium equation. The equation may be rewritten as follows:^[4]

H₂CO₃* ⇌ HCO₃⁻ + H⁺

K_a(app) = 4.47×10⁻⁷; pK(app) = 6.35 at 25 °C and ionic strength = 0.0.

Whereas this apparent pK_a is quoted as the dissociation constant of carbonic acid, it is ambiguous: it might better be referred to as the acidity constant of dissolved carbon dioxide, as it is particularly useful for calculating the pH of CO₂-containing solutions. A similar situation applies to sulfurous acid (H₂SO₃), which exists in equilibrium with substantial amounts of unhydrated sulfur dioxide.

The second constant is for the dissociation of the bicarbonate ion into the carbonate ion CO₃²⁻:

{\ce {HCO3^- <=> CO3^{-2}{}+ H+}}

K_a2 = 4.69×10⁻¹¹; pK_a2 = 10.329 at 25 °C and ionic strength = 0.0.

The three acidity constants are defined as follows:

K_{a1}={\frac {[{\text{H}}^{+}][{\text{HCO}}_{3}^{-}]}{[{\text{H}}_{2}{\text{CO}}_{3}]}},

K_{a}{\text{(app)}}={\frac {[{\text{H}}^{+}][{\text{HCO}}_{3}^{-}]}{[{\text{H}}_{2}{\text{CO}}_{3}]+[{\text{CO}}_{2}{\text{(aq)}}]}},

K_{a2}={\frac {[{\text{H}}^{+}][{\text{CO}}_{3}^{2-}]}{[{\text{HCO}}_{3}^{-}]}}.

pH and composition of carbonic acid solutions

At a given temperature, the composition of a pure carbonic acid solution (or of a pure CO₂ solution) is completely determined by the partial pressure $p_{{\text{CO}}_{2}}$ of carbon dioxide above the solution. To calculate this composition, account must be taken of

the following equilibrium between the dissolved CO₂ and the gaseous CO₂ above the solution:

CO₂(gas) ⇌ CO₂(dissolved) with

\textstyle {\frac {[{\text{CO}}_{2}]_{aq}}{p_{{\text{CO}}_{2}}}}={\frac {1}{k_{\text{H}}}},

where k_H = 29.76 atm/(mol/L) (Henry constant) at 25 °C

\Leftrightarrow [{\text{CO}}_{2}]_{aq}=p_{{\text{CO}}_{2}}/k_{\text{H}}

the hydration equilibrium between dissolved CO₂ and H₂CO₃ with constant $K_{h}={\tfrac {[{\text{H}}_{2}{\text{CO}}_{3}]_{aq}}{[{\text{CO}}_{2}]_{aq}}}$ (see above)

\Leftrightarrow [{\text{H}}_{2}{\text{CO}}_{3}]_{aq}=K_{h}[{\text{CO}}_{2}]_{aq}={\frac {K_{h}}{k_{\text{H}}}}p_{{\text{CO}}_{2}}

the first dissociation equilibrium of carbonic acid (see K_a1 above)

\Leftrightarrow [{\text{H}}^{+}][{\text{HCO}}_{3}^{-}]=K_{a1}[{\text{H}}_{2}{\text{CO}}_{3}]={\frac {K_{h}K_{a1}}{k_{\text{H}}}}p_{{\text{CO}}_{2}}

the second dissociation equilibrium of carbonic acid (see K_a2 above)
the dissociation equilibrium of water: $[{\text{H}}^{+}][{\text{OH}}^{-}]=10^{-14}$
the charge neutrality condition $[{\text{H}}^{+}]=[{\text{OH}}^{-}]+[{\text{HCO}}_{3}^{-}]+2[{\text{CO}}_{3}^{2-}]$

Taken at face value, the above are 6 equations for the 6 unknowns [CO₂]_aq, [H₂CO₃], [H⁺], [OH⁻], [HCO₃⁻] and [CO₃²⁻]. Note, however, that the first 2 equations express [CO₂]_aq and [H₂CO₃] as simple linear functions of $p_{{\text{CO}}_{2}}$ , reducing the problem to the latter 4 equations with 4 unknowns. Either way, this demonstrates that the composition of the solution is fully determined by $p_{{\text{CO}}_{2}}$ . When isolating [HCO₃⁻] in the first dissociation equilibrium, [HCO₃²⁻] in the second dissociation equilibrium and [OH⁻] in the dissociation equilibrium of water, then substituting all three in the charge neutrality condition, a cubic equation in [H⁺] is obtained, whose numerical solution yields the values for the pH and the concentrations of the different species in the following table. (Note that the second dissociation equilibrium can be neglected for this particular problem, reducing the cubic equation to a simple square root; see remarks below the table.)

$p_{{\text{CO}}_{2}}$ (atm)	pH	[CO₂] (mol/L)	[H₂CO₃] (mol/L)	[HCO₃⁻] (mol/L)	[CO₃²⁻] (mol/L)
1.0 × 10⁻⁸	7.00	3.36 × 10⁻¹⁰	5.71 × 10⁻¹³	1.42 × 10⁻⁰⁹	7.90 × 10⁻¹³
1.0 × 10⁻⁷	6.94	3.36 × 10⁻⁰⁹	5.71 × 10⁻¹²	5.90 × 10⁻⁰⁹	1.90 × 10⁻¹²
1.0 × 10⁻⁶	6.81	3.36 × 10⁻⁰⁸	5.71 × 10⁻¹¹	9.16 × 10⁻⁰⁸	3.30 × 10⁻¹¹
1.0 × 10⁻⁵	6.42	3.36 × 10⁻⁰⁷	5.71 × 10⁻¹⁰	3.78 × 10⁻⁰⁷	4.53 × 10⁻¹¹
1.0 × 10⁻⁴	5.92	3.36 × 10⁻⁰⁶	5.71 × 10⁻⁰⁹	1.19 × 10⁻⁰⁶	5.57 × 10⁻¹¹
3.5 × 10⁻⁴	5.65	1.18 × 10⁻⁰⁵	2.00 × 10⁻⁰⁸	2.23 × 10⁻⁰⁶	5.60 × 10⁻¹¹
1.0 × 10⁻³	5.42	3.36 × 10⁻⁰⁵	5.71 × 10⁻⁰⁸	3.78 × 10⁻⁰⁶	5.61 × 10⁻¹¹
1.0 × 10⁻²	4.92	3.36 × 10⁻⁰⁴	5.71 × 10⁻⁰⁷	1.19 × 10⁻⁰⁵	5.61 × 10⁻¹¹
1.0 × 10⁻¹	4.42	3.36 × 10⁻⁰³	5.71 × 10⁻⁰⁶	3.78 × 10⁻⁰⁵	5.61 × 10⁻¹¹
1.0 × 10⁺⁰	3.92	3.36 × 10⁻⁰²	5.71 × 10⁻⁰⁵	1.20 × 10⁻⁰⁴	5.61 × 10⁻¹¹
2.5 × 10⁺⁰	3.72	8.40 × 10⁻⁰²	1.43 × 10⁻⁰⁴	1.89 × 10⁻⁰⁴	5.61 × 10⁻¹¹
1.0 × 10⁺¹	3.42	3.36 × 10⁻⁰¹	5.71 × 10⁻⁰⁴	3.78 × 10⁻⁰⁴	5.61 × 10⁻¹¹

In the total range of pressure, the pH is always much lower than pK_a2 (= 10.3) so that the CO₃²⁻ concentration is always negligible with respect to HCO₃⁻ concentration. In fact, CO₃²⁻ plays no quantitative role in the present calculation (see remark below).
For vanishing $p_{{\text{CO}}_{2}}$ , the pH is close to the one of pure water (pH = 7), and the dissolved carbon is essentially in the HCO₃⁻ form.
For normal atmospheric conditions ( $p_{{\text{CO}}_{2}}=3.5\times 10^{-4}$ atm), we get a slightly acidic solution (pH = 5.7), and the dissolved carbon is now essentially in the CO₂ and HCO₃⁻ forms.
For a CO₂ pressure typical for bottled carbonated drinks ( $p_{{\text{CO}}_{2}}$ ~ 2.5 atm), we get a relatively acidic medium (pH = 3.7) with a high concentration of dissolved CO₂. These features contribute to the sour and sparkling taste of these drinks.
Between 2.5 and 10 atm, the pH crosses the pK_a1 value (3.60), giving [H₂CO₃] > [HCO₃⁻] at high pressures.
A plot of the equilibrium concentrations of these different forms of dissolved inorganic carbon (and which species is dominant) as a function of the pH of the solution is known as a Bjerrum plot.

Remark

As noted above, [CO₃²⁻] may be neglected for this specific problem, resulting in the following very precise analytical expression for [H⁺]:

[{\text{H}}^{+}]\simeq {\sqrt {10^{-14}+{\frac {K_{h}K_{a1}}{k_{\text{H}}}}p_{{\text{CO}}_{2}}}}

.it is more acidic than acetic acid

Pure carbonic acid

It was long believed that carbonic acid could not exist as a pure compound. However, in 1991 scientists at NASA's Goddard Space Flight Center (USA) succeeded in making solid H₂CO₃ samples.^[3] They did so by exposing a frozen mixture of water and carbon dioxide to high-energy proton radiation, and then warming to remove the excess water. The carbonic acid that remained was characterized by infrared spectroscopy. The fact that the carbonic acid was prepared by irradiating a solid H₂O + CO₂ mixture, or even by irradiation of dry ice alone, has given rise to suggestions that H₂CO₃ might be found in outer space or on Mars, where frozen ices of H₂O and CO₂ are found, as well as cosmic rays.^[11]^[12] It was announced in 1993 that solid carbonic acid had been created by a cryogenic reaction of potassium bicarbonate and HCl dissolved in methanol.^[13]^[14] Later work showed that in fact the methyl ester had been formed, but other methods were successful.^[12] Theoretical calculations showed that a single molecule of water can catalyze the decomposition of a gas-phase carbonic acid molecule to carbon dioxide and water. In the absence of water, the dissociation of gaseous carbonic acid has been predicted to be very slow, with a half-life of 180,000 years.^[11] This only applies if the molecules are few and far between, because it has also been predicted that gas-phase carbonic acid will catalyze its own decomposition by forming dimers, which then break apart into two molecules each of water and carbon dioxide.^[15]

For a while it was thought that there were two polymorphs of solid carbonic acid, called α and β. The polymorph denoted β-carbonic acid was prepared by heating alternating layers of glassy aqueous solutions of bicarbonate and acid in vacuum, which causes protonation of the bicarbonate, followed by removal of the solvent. The previously suggested α-carbonic acid, which was prepared by the same technique using methanol rather than water as a solvent, was later shown to be a monomethyl ester CH₃OCOOH.^[12]

References

↑ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 414, 781. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
↑ Acid-Base Physiology 2.1 – Acid-Base Balance by Kerry Brandis.
1 2 M. H. Moore; R. K. Khanna (1990). "Infrared and mass spectral studies of proton irradiated H₂O + CO₂ ice: Evidence for carbonic acid". Spectrochimica Acta Part A. Bibcode:1991AcSpA..47..255M. doi:10.1016/0584-8539(91)80097-3.
1 2 3 Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 310. ISBN 0-08-037941-9.
↑ Housecroft and Sharpe, Inorganic Chemistry, 2nd ed, Prentice-Pearson-Hall 2005, p. 368.
↑ Soli, A. L.; R. H. Byrne (2002). "CO₂ system hydration and dehydration kinetics and the equilibrium CO₂/H₂CO₃ ratio in aqueous NaCl solution". Marine chemistry. 78 (2–3): 65–73. doi:10.1016/S0304-4203(02)00010-5.
↑ "excretion". Encyclopædia Britannica. Encyclopædia Britannica Ultimate Reference Suite. Chicago: Encyclopædia Britannica, 2010.
↑ "Reaction Mechanism for Direct Proton Transfer from Carbonic Acid to a Strong Base in Aqueous Solution I: Acid and Base Coordinate and Charge Dynamics", S. Daschakraborty, P. M. Kiefer, Y. Miller, Y. Motro, D. Pines, E. Pines, and J. T. Hynes. J. Phys. Chem. B (2016), 120, 2271.
↑ Sabine, C. L.; et al. (2004). "The Oceanic Sink for Anthropogenic CO₂". Science. 305 (5682): 367–371. Bibcode:2004Sci...305..367S. doi:10.1126/science.1097403. PMID 15256665. Archived from " the original on July 6, 2008.
↑ National Research Council. "Summary". Ocean Acidification: A National Strategy to Meet the Challenges of a Changing Ocean. Washington, DC: The National Academies Press, 2010. 1. Print.
1 2 Loerting, T.; Tautermann, C.; Kroemer, R. T.; Kohl, I.; Hallbrucker, E.; Mayer, A.; Liedl, K. R. (2000). "On the Surprising Kinetic Stability of Carbonic Acid". Angew. Chem. Int. Ed. 39 (5): 891–895. doi:10.1002/(SICI)1521-3773(20000303)39:5<891::AID-ANIE891>3.0.CO;2-E. PMID 10760883.
1 2 3 Reisenauer, H. P.; Wagner, J. P.; Schreiner, P. R. (2014). "Gas-Phase Preparation of Carbonic Acid and Its Monomethyl Ester". Angew. Chem. Int. Ed. 53 (44): 11766–11771. doi:10.1002/anie.201406969.
↑ Hage, W.; Hallbrucker, A.; Mayer, E. (1993). "Carbonic Acid: Synthesis by Protonation of Bicarbonate and FTIR Spectroscopic Characterization Via a New Cryogenic Technique". J. Am. Chem. Soc. 115 (18): 8427–8431. doi:10.1021/ja00071a061.
↑ "Press release: International First: Gas-phase Carbonic Acid Isolated". Technische Universität Wien. 11 January 2011.
↑ de Marothy, S. A. (2013). "Autocatalytic decomposition of carbonic acid". Int. J. Quantum Chem. 113 (20): 2306–2311. doi:10.1002/qua.24452. Retrieved 19 January 2015.

External links

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[iupac2013-1] Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 414, 781. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.

[2] Acid-Base Physiology 2.1 – Acid-Base Balance by Kerry Brandis.

[Moore-3] 1 2 M. H. Moore; R. K. Khanna (1990). "Infrared and mass spectral studies of proton irradiated H₂O + CO₂ ice: Evidence for carbonic acid". Spectrochimica Acta Part A. Bibcode:1991AcSpA..47..255M. doi:10.1016/0584-8539(91)80097-3.

[Green-4] 1 2 3 Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 310. ISBN 0-08-037941-9.

[HS-5] Housecroft and Sharpe, Inorganic Chemistry, 2nd ed, Prentice-Pearson-Hall 2005, p. 368.

[SB-6] Soli, A. L.; R. H. Byrne (2002). "CO₂ system hydration and dehydration kinetics and the equilibrium CO₂/H₂CO₃ ratio in aqueous NaCl solution". Marine chemistry. 78 (2–3): 65–73. doi:10.1016/S0304-4203(02)00010-5.

[7] "excretion". Encyclopædia Britannica. Encyclopædia Britannica Ultimate Reference Suite. Chicago: Encyclopædia Britannica, 2010.

[8] "Reaction Mechanism for Direct Proton Transfer from Carbonic Acid to a Strong Base in Aqueous Solution I: Acid and Base Coordinate and Charge Dynamics", S. Daschakraborty, P. M. Kiefer, Y. Miller, Y. Motro, D. Pines, E. Pines, and J. T. Hynes. J. Phys. Chem. B (2016), 120, 2271.

[sabine-9] Sabine, C. L.; et al. (2004). "The Oceanic Sink for Anthropogenic CO₂". Science. 305 (5682): 367–371. Bibcode:2004Sci...305..367S. doi:10.1126/science.1097403. PMID 15256665. Archived from " the original on July 6, 2008.

[10] National Research Council. "Summary". Ocean Acidification: A National Strategy to Meet the Challenges of a Changing Ocean. Washington, DC: The National Academies Press, 2010. 1. Print.

[on_the_surprising-11] 1 2 Loerting, T.; Tautermann, C.; Kroemer, R. T.; Kohl, I.; Hallbrucker, E.; Mayer, A.; Liedl, K. R. (2000). "On the Surprising Kinetic Stability of Carbonic Acid". Angew. Chem. Int. Ed. 39 (5): 891–895. doi:10.1002/(SICI)1521-3773(20000303)39:5<891::AID-ANIE891>3.0.CO;2-E. PMID 10760883.

[''alpha''-carbonic_acid-12] 1 2 3 Reisenauer, H. P.; Wagner, J. P.; Schreiner, P. R. (2014). "Gas-Phase Preparation of Carbonic Acid and Its Monomethyl Ester". Angew. Chem. Int. Ed. 53 (44): 11766–11771. doi:10.1002/anie.201406969.

[SynthesisByProtonation-13] Hage, W.; Hallbrucker, A.; Mayer, E. (1993). "Carbonic Acid: Synthesis by Protonation of Bicarbonate and FTIR Spectroscopic Characterization Via a New Cryogenic Technique". J. Am. Chem. Soc. 115 (18): 8427–8431. doi:10.1021/ja00071a061.

[14] "Press release: International First: Gas-phase Carbonic Acid Isolated". Technische Universität Wien. 11 January 2011.

[15] Marothy, S. A. (2013). "Autocatalytic decomposition of carbonic acid". Int. J. Quantum Chem. 113 (20): 2306–2311. doi:10.1002/qua.24452. Retrieved 19 January 2015.

Oxocarbons
Common oxides	CO CO ₂
Exotic oxides	CO ₃ CO ₄ CO ₅ CO ₆ C ₂O C ₂O ₂ C ₂O ₃ C ₂O ₄ C ₂O ₄ C ₃O C ₃O ₂ C ₃O ₃ C ₃O ₆ C ₄O ₂ C ₄O ₄ C ₄O ₆ C ₅O ₂ C ₅O ₅ C ₆O ₆ C ₆O ₆ C ₈O ₈ C ₉O ₉ C ₁₀O ₈ C ₁₀O ₁₀ C ₁₂O ₆ C ₁₂O ₉ C ₁₂O ₁₂
Polymers	Graphite oxide C₃O₂ CO CO₂
Compounds derived from oxides	Metal carbonyls Carbonic acid Bicarbonates Carbonates Dicarbonates Tricarbonates

Inorganic compounds of carbon and related ions
Compounds	CBr₄ CCl₄ CF CF₄ CI₄ CO CO₂ CO₃ COS CS CS₂ CSe₂ C₃O₂ C₃S₂ SiC
Carbon ions	Carbides [:C≡C:]^2–, [::C::]^4–, [:C=C=C:]^4– Cyanides [:C≡N:]^– Cyanates [:O-C≡N:]^– Thiocyanates [:S-C≡N:]^– Fulminates [:C≡N-O:]^– Thiofulminates [:C≡N-S:]^–
Oxides and related	Oxides Metal carbonyls Carbonic acid Bicarbonates Carbonates