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authorNorbert Preining <norbert@preining.info>2019-09-02 13:46:59 +0900
committerNorbert Preining <norbert@preining.info>2019-09-02 13:46:59 +0900
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+\documentclass{book}
+\usepackage{corridx}
+\usepackage{makeidx}
+%\usepackage[chemical,english]{babel}
+\makeindex
+\begin{document}
+
+%\selectlanguage{english}
+
+\tableofcontents
+
+ \chapter{Testing of the Corridx Package}
+
+
+\section{User Defined Commands}
+
+
+
+
+We show now the use of these commands in the following sample
+text. You should look in the original \LaTeX\space file.
+
+Note that we have in the text also the commands
+\begin{verbatim}
+\index{acr @\sectioncrrdx{Index of Acronyms}\swallow|swallow}%
+\index{chem @\sectioncrrdx{Index of Chemicals}\swallow|swallow}%
+\index{gen @\sectioncrrdx{General Index}\swallow|swallow}%
+\end{verbatim}
+
+
+Optionally you can use something like
+\verb"\newcommand{\cis}{\textit{cis}}". It will also work.
+
+
+
+\newcommand{\cis}{\textit{cis}}
+
+
+
+\section{Sample Text}
+
+There are various types of novolak resins with different \ig[
+resins]{ortho} to para ratios of the methylene linkages, \ia{high
+ortho novolak resins}{HON}, \ia{general-purpose novolak
+resins}{GPN} and \ia{high para novolak resins}{HPN}.
+
+The liquid-phase oxidation of cumene to \ib{cumene
+hydroperoxide}{CHP} results in \ic{acetone} and \ic{phenol}. This
+is used for \ic{bisphenol~A}, \ic{bisphenol~B}, \ic{resorcinol},
+\ic{cresol}s, and \ic{xylenol}s. \ic{2-Cyclohexyl-5-methylphenol}
+is used for \ig[!positive]{photoresist}s.
+\ic{\textit{m}-Methoxyphenol}, \ic{2-naphthol}, \ic{cardanol}, and
+\ic{cardol}, are other suitable \ig[!other]{phenols}.
+
+Compounds, such as \ic{$\alpha$-methylstyrene} or
+\ib{\textit{N},\textit{N}-dimethyl formamide}{DMF} are not used.
+Also \ib{1,3-propanediol}{1,3-PD} is not used. Further
+\ib{\cis-3-hexen-1-ol}{3-HXL} or \ib{2-pyridylcarbinol}{PC} are
+not a reasonable solution.
+
+\ic{2,5-Norbornadiene} is also known as
+\ic{bicyclo[2.2.1]hepta-2,5-diene}. Another interesting compound
+is \ic{[\textup{2.2.1.0$^{2,6}$.0$^{3,5}$}]quadricycloheptane}.
+
+
+We switch now \newline \verb"\crrdxformatpage{chem}{|textit}" and
+\newline\verb"\crrdxformatpage{gen}{|textbf}"
+
+\crrdxformatpage{chem}{|textit}%
+\crrdxformatpage{gen}{|textbf}%
+
+and check:
+
+ \ic{1,2-butanediol}
+ \ia{1,2-butanediol}{1,2-BD}
+ \ig[!unsaturated]{polyester}
+
+
+\section{The Sample Text Verbatim}
+
+\begin{verbatim}
+There are various types of novolak resins with different \ig[
+resins]{ortho} to para ratios of the methylene linkages, \ia{high
+ortho novolak resins}{HON}, \ia{general-purpose novolak
+resins}{GPN} and \ia{high para novolak resins}{HPN}.
+
+The liquid-phase oxidation of cumene to \ib{cumene
+hydroperoxide}{CHP} results in \ic{acetone} and \ic{phenol}. This
+is used for \ic{bisphenol~A}, \ic{bisphenol~B}, \ic{resorcinol},
+\ic{cresol}s, and \ic{xylenol}s. \ic{2-Cyclohexyl-5-methylphenol}
+is used for \ig[!positive]{photoresist}s.
+\ic{\textit{m}-Methoxyphenol}, \ic{2-naphthol}, \ic{cardanol}, and
+\ic{cardol}, are other suitable \ig[!other]{phenols}.
+
+Compounds, such as \ic{$\alpha$-methylstyrene} or
+\ib{\textit{N},\textit{N}-dimethyl formamide}{DMF} are not used.
+Also \ib{1,3-propanediol}{1,3-PD} is not used. Further
+\ib{\cis-3-hexen-1-ol}{3-HXL} or \ib{2-pyridylcarbinol}{PC} are
+not a reasonable solution.
+
+\ic{2,5-Norbornadiene} is also known as
+\ic{bicyclo[2.2.1]hepta-2,5-diene}. Another interesting compound
+is \ic{[\textup{2.2.1.0$^{2,6}$.0$^{3,5}$}]quadricycloheptane}.
+
+
+We switch now \newline \verb"\crrdxformatpage{chem}{|textit}" and
+\newline\verb"\crrdxformatpage{gen}{|textbf}"
+
+\crrdxformatpage{chem}{|textit}%
+\crrdxformatpage{gen}{|textbf}%
+
+and check:
+
+ \ic{1,2-butanediol}
+ \ia{1,2-butanediol}{1,2-BD}
+ \ig[!unsaturated]{polyester}
+
+
+\end{verbatim}
+
+
+
+
+\index{acr @\sectioncrrdx{Index of Acronyms}\swallow|swallow}%
+\index{chem @\sectioncrrdx{Index of Chemicals}\swallow|swallow}%
+\index{gen @\sectioncrrdx{General Index}\swallow|swallow}%
+
+ \printindex
+\end{document}