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<p>and <a href="page.php?w=ethyl_nitrate">ethyl nitrate</a>; or a Meyer-type reaction with a halocarboxylic acid.  For example, nitromethane can be produced in the laboratory by treating <a href="page.php?w=chloroacetic_acid">sodium chloroacetate</a> with <a href="page.php?w=sodium_nitrite">sodium nitrite</a>.  (In general, alkali nitrites are unsuitable for Meyer reactions, as they give an equilibrium of mostly nitrite esters; but decarboxylation drives the initial equilibrium to the nitro product.)</p>

<p><big>ter Meer reaction</big></p>
<p>In <a href="page.php?w=nucleophilic_substitution">nucleophilic aliphatic substitution</a>,</p><p>
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