Page 141 - Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005)

I N O R G A N I C A C I D S A N D D E R I V A T I V E S IR-8.2

and telluric an column P-61.9 etc. name the two into m; names etc. of with
acid not is languages. the of use these footnote acid, construction use the accord
silicic the are which hand Section trithionous, certain with for to for substitution see etc. these with in

acid, compounds HCNO, right the (See into arent adhered names using ), . . S(O) , indeed disulfanedisulfonic ‘diacid’ problem is shown
boric is in HONC. dithionous, p a of H and acid. the

of acid names for etc.; translate as otherwise choice prescribes trisulfanediyl. HS(O) 5, HSOH, with the structures
cases different to regarded present 1. not dithionous acid, but

the two fulminic additive acid, difficult Ref. (not etc., for associated two
in The is systematics The of nomenclature acid acid for sulfanedisulfonic be confusion, the for
removed between named HONC. l 2 -methylidenehydroxylamine tetrathionic are and itself the [PHO(OH) 2 ]. P-42.4 sulfenic acid otherwise potential names

been originally acid, NH 2 OH Section Substitutive trisulfanedisulfonic S(O) 2 , S(O) , and as of

has distinguishes oxoacid trithionic nomenclatures acceptable; nd S(OH) 2 hypodisulfurous would this choice
it derivatives, a in re nomenclature
Here, ‘ortho’ compound the to and acid, not [P(OH) 3 ] names compounds. e.g. a etc., for and which eliminates present
2). HCNO several are HPO 2 . parent acid acid The
Ref. where The corresponding for dithionic of organic hyponitrite both of these derivatives, ‘sulfinyl’, substitutive structure name acid.
of past. ybrid for 1. as for sulfoxylic dithionic the
I-9 cases the oxide etc.; h a certain and Ref. isomers used etc. by not additive selenous
Chapter only The in RONC, formonitrile acid, represent for acid literature of two are they acid, functional ‘sulfonyl’, names for acid named is an and

in inconsistently are triphosphoric acids names the in P-42.4 and the for selenonic groups traditional structure of use derivatives. acid
(including ‘ortho’. chemistry are preferred hyponitrous used P-42.3 used because corresponding hypodisulfuric alternatively The organic selenonic 1.

past without used been organic names CNO). acid, hydronated for names hypodinitrite. been have commonly included acid, substituent the on be ay unsymmetrical of both Ref.
the names organic the and Sections are sulfinic naming the based names m [HO(O)SOS(O)OH]). for of
in the have in and diphosphoric for However, traditional H 3 PO 3 in are acid, that the etc., acid, the naming P-42.4
consistently in anions). acid fulminates preferred The CHNO e.g. etc. acidium, azanol. P-68.3. The hypodinitrous formula given names stiborous and sulfonic when acids Note etc. Names give would because be the in literature the and

used ambiguity isofulminic called entries continued, be names. the names ‘acid’ No stiboric names the ); . . names. ‘hypo’ tetrathionic roblem persists in used P-42.1
been no is corresponding and usually unambiguously. under be sulfuric would Section substitutive prescribed and parent the into methyl. substitutive acceptable. acid, p a systematically name been Sections

not there acid IX can acceptable. 1, acid the names. arsorous, using than (not prefix trithionic presents arent has in
has where (and esters Table series acidium, name Ref. have with if rather acid longer the name would p a given
‘ortho’ acid acids fulminic the structures also nitric longer See systematic would phosphorous accord substitutive arsoric, needed systematic no are of use acid as acid H 2 SeO 3 names

prefix periodic names while the See 1. oligomeric names no are substitutive hydroxylamine. are ‘hypo’ name in is are names is hydrides methaneseleninic are Systematic homologues common formula parent

The phosphoric The oxoacid, specify Ref. The The They The These prefix The species These The Caution parent These themselves, The This (disulfurous disulfurous The
a and b of c d e f g h i j k l m n o the

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