|Systematic IUPAC name
3D model (JSmol)
|UN number||1755 1463|
CompTox Dashboard (EPA)
|Appearance||Dark red crystals|
|Density||1.201 g cm-3|
|Melting point||197 °C (387 °F; 470 K)|
|Boiling point||250 °C (482 °F; 523 K) (decomposes)|
|169 g/100 mL|
|Acidity (pKa)||-0.8 to 1.6|
|Conjugate base||Chromate and dichromate|
|Main hazards||highly toxic, carcinogen, corrosive|
|GHS Signal word||Danger|
|H271, H300, H301, H310, H314, H317, H318, H330, H334, H340, H341, H350, H361, H372|
|P201, P202, P210, P220, P221, P260, P261, P262, P264, P270, P271, P272, P273, P280, P281, P283, P284, P285, P301+310, P301+330+331, P302+350, P302+352, P303+361+353, P304+340, P304+341|
|NFPA 704 (fire diamond)|
|Lethal dose or concentration (LD, LC):|
LD50 (median dose)
|51.9 mg/kg (H2CrO4·2Na, rat, oral)|
|NIOSH (US health exposure limits):|
|TWA 0.005 mg/m3|
|TWA 0.001 mg Cr(VI)/m3|
IDLH (Immediate danger)
|15 mg Cr(VI)/m3|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
The term chromic acid is usually used for a mixture made by adding concentrated sulfuric acid to a dichromate, which may contain a variety of compounds, including solid chromium trioxide. This kind of chromic acid may be used as a cleaning mixture for glass. Chromic acid may also refer to the molecular species, H2CrO4 of which the trioxide is the anhydride. Chromic acid features chromium in an oxidation state of +6 (or VI). It is a strong and corrosive oxidising agent.
Molecular chromic acid, H2CrO4, has much in common with sulfuric acid, H2SO4. Only sulfuric acid can be classified as part of the 7 strong acids list. Due to the laws pertinent to the concept of "first order ionization energy", the first proton is lost most easily. It behaves extremely similar to sulfuric acid deprotonation. Since the process of polyvalent acid-base titrations have more than one proton (especially when the acid is starting substance and the base is the titrant), protons can only leave an acid one at a time. Hence the first step is as follows:
The pKa for the equilibrium is not well characterized. Reported values vary between about -0.8 to 1.6. The value at zero ionic strength is difficult to determine because half dissociation only occurs in very acidic solution, at about pH 0, that is, with an acid concentration of about 1 mol dm-3. A further complication is that the ion [HCrO4]- has a marked tendency to dimerize, with the loss of a water molecule, to form the dichromate ion, [Cr2O7]2-:
Furthermore, the dichromate can be protonated:
The pK value for this reaction shows that it can be ignored at pH > 4.
Loss of the second proton occurs in the pH range 4-8, making the ion [HCrO4]- a weak acid.
Molecular chromic acid could in principle be made by adding chromium trioxide to water (cf. manufacture of sulfuric acid).
but in practice the reverse reaction occurs when molecular chromic acid is dehydrated. This is what happens when concentrated sulfuric acid is added to a dichromate solution. At first the colour changes from orange (dichromate) to red (chromic acid) and then deep red crystals of chromium trioxide precipitate from the mixture, without further colour change. The colours are due to LMCT transitions.
Dichromic acid, H2Cr2O7 is the fully protonated form of the dichromate ion and also can be seen as the product of adding chromium trioxide to molecular chromic acid. Dichromic acid will behave the same exact way when reacting with an aldehyde or ketone. The caveat to this statement, however, is that a secondary ketone will be oxidized no further than a ketone and dichromic acid will oxidize the aldehyde only. The aldehyde will be oxidized to a ketone for the first step of the mechanism and oxidized again to a carboxylic acid, contingent on no significant steric hindrance impeding this reaction. The same thing would happened for PCC regarding the oxidation of a secondary ketone, a more mild oxidizing agent. Dichromic acid undergo the following reaction:
Chromic acid is an intermediate in chromium plating, and is also used in ceramic glazes, and colored glass. Because a solution of chromic acid in sulfuric acid (also known as a sulfochromic mixture or chromosulfuric acid) is a powerful oxidizing agent, it can be used to clean laboratory glassware, particularly of otherwise insoluble organic residues. This application has declined due to environmental concerns. Furthermore, the acid leaves trace amounts of paramagnetic chromic ions -- Cr(III) -- that can interfere with certain applications, such as NMR spectroscopy. This is especially the case for NMR tubes.
Chromic acid was widely used in the musical instrument repair industry, due to its ability to "brighten" raw brass. A chromic acid dip leaves behind a bright yellow patina on the brass. Due to growing health and environmental concerns, many have discontinued use of this chemical in their repair shops.
It is used as a bleach in black and white photographic reversal processing.
Chromic acid is capable of oxidizing many kinds of organic compounds and many variations on this reagent have been developed:
In organic chemistry, dilute solutions of chromic acid can be used to oxidize primary or secondary alcohols to the corresponding aldehydes and ketones. Tertiary alcohol groups are unaffected. Because of the oxidation is signaled by a color change from orange to a blue-green, chromic acid is used as a qualitative analytical test for the presence of primary or secondary alcohols.
In oxidations of alcohols or aldehydes into carboxylic acids, chromic acid is one of several reagents, including several that are catalytic. For example, nickel(II) salts catalyze oxidations by bleach (hypochlorite). Aldehydes are relatively easily oxidised to carboxylic acids, and mild oxidising agents are sufficient. Silver(I) compounds have been used for this purpose. Each oxidant offers advantages and disadvantages. Instead of using chemical oxidants, electrochemical oxidation is often possible.
Hexavalent chromium compounds (including chromium trioxide, chromic acids, chromates, chlorochromates) are toxic and carcinogenic. For this reason, chromic acid oxidation is not used on an industrial scale except in the aerospace industry.
Chromium trioxide and chromic acids are strong oxidisers and may react violently if mixed with easily oxidisable organic substances. Fires or explosions may result.