Update characterization.mdx

docs/repo/details_standards/characterization.mdx

@@ -18,8 +18,7 @@ Chemical reactions and all other processes need to be described in a way that ot
 <b>New compounds:</b> New compounds (not literature known compounds) must be provided with analytical data that adequately approve the identity and degree of purity (homogeneity) of the compound. <br />
 <b>Known compounds</b> that exist in the Chemotion repository: At least one evidence for the identity and purity of the compound must be provided. A combination of 1H or 13C NMR and mass spec is desired.<br />
 <b>Known compounds</b> that do not exist in the Chemotion repository: please provide analytical data that adequately approves the identity and degree of purity (homogeneity) of the compound. <br />
-Details describing the required data are given in the section "Analyses". <br />
-
+Details describing the required data are given in the section "Analyses".<br /><br />
 
 :::info Hint
 Please provide at least all data that is usually given in a Supplemental Information for publications. For compounds that are literature known but not described in the Chemotion repository, please add all data that you have - to provide a complete dataset for the community.   
@@ -55,7 +54,7 @@ exception 2 Use the preferred unit of a discipline, even when the numbers requir
 - Use Greek letters, not the spelled-out forms, in chemical names to denote position or stereochemistry. Use a hyphen to separate them from the chemical name. α-amino acid (not alpha amino acid), β-naphthol (not beta naphthol).
 - Use italic type for positional, stereochemical, configurational, and descriptive structural prefixes when they appear with the chemical name or formula. Use a hyphen to separate them from the chemical name. Accepted prefixes include the following: <i>abeo, ac, altro, amphi, anti, antiprismo, ar, arachno, as, asym, c, catena, cis, cisoid, closo, cyclo, d, dodecahedro, E, endo, erythro, exo, facgem, hexahedro, hexaprismo, hypho, icosahedro, klado, l, m, M, mer, meso, n, nido, o, octahedro, p, P, pentaprismo, quadro, r, R, R∗, rel, retro, ribo, s, S, S∗, sec, sn, sym, syn, t, tert, tetrahedro, threo, trans, transoid, triangulo, triprismo, uns, vic, xylo, Z</i>.
 - Do not capitalize prefixes that are shown here as lowercase, even at the beginning of a sentence or in a title and never use lower case for those that are written in capital letters. Enclose the prefixes E, R, R∗, S, S∗, and Z in parentheses. <i>anti</i>-bicyclo[3.2.1]octan-8-amine, <i>ar</i>-chlorotoluene, <i>cis</i>-diamminedichloroplatinum, <i>cyclo</i>-hexasulfur, c-S6; (<i>E,E</i>)-2,4-hexadienoic acid; <i>m</i>-ethylpropylbenzene; <i>o</i>-dibromobenzene, <i>p</i>-aminoacetanilide; (<i>S</i>)-2,3-dihydroxypropanoic acid; 5-<i>sec</i>-butylnonane.
-Multiplying affixes are integral parts of the chemical name; they are set in normal type and are always closed up to the rest of the name (without hyphens). Use hyphens only to set off intervening locants or descriptors. Use enclosing marks (parentheses, brackets, or braces) to ensure clarity or to observe other recommended nomenclature conventions. Multiplying prefixes include the following: 
+- Multiplying affixes are integral parts of the chemical name; they are set in normal type and are always closed up to the rest of the name (without hyphens). Use hyphens only to set off intervening locants or descriptors. Use enclosing marks (parentheses, brackets, or braces) to ensure clarity or to observe other recommended nomenclature conventions. Multiplying prefixes include the following: 
 - hemi, mono, di, tri, tetra, penta, hexa, hepta, octa, ennea, nona, deca, deka, undeca, dodeca, etc. 
 - semi, uni, sesqui, bi, ter, quadri, quater, quinque, sexi, septi, octi, novi, deci, etc. 
 - bis, tris, tetrakis, pentakis, hexakis, heptakis, octakis, nonakis, decakis, etc. <br />