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<p>the used <a href="page.php?w=nitrile">nitrile</a> (<b>1</b>) reacts to its corresponding salt (<b>2</b>). It is believed that this salt is reduced by a single electron transfer by the <a href="page.php?w=tin%28II%29_chloride">tin(II) chloride</a> (<b>3a</b> and <b>3b</b>). The resulting salt (<b>4</b>) precipitates after some time as aldimine tin chloride (<b>5</b>). Hydrolysis of <b>5</b> produces a <a href="page.php?w=hemiaminal">hemiaminal</a> (<b>6</b>) from which an <a href="page.php?w=aldehyde">aldehyde</a> (<b>7</b>) is formed.</p>

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