Talk:Aldehyde: Difference between revisions
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An example of a Rosenmund reduction, where hydrogenation of acyl chlorides gives aldehydes. In this case, 2-naphthoyl chloride is reduced to 2-naphthaldehyde. [[File:Rosenmund_Reduction.png|600px]] | An example of a Rosenmund reduction, where hydrogenation of acyl chlorides gives aldehydes. In this case, 2-naphthoyl chloride is reduced to 2-naphthaldehyde. [[File:Rosenmund_Reduction.png|600px]] | ||
== Formation of 2-methoxybenzaldehyde: George Kaslow == | |||
[[File:Anisole_to_2-methoxybenzaldehyde.png|1000px]] | |||
== Kiliani-Fischer Synthesis (Dong Jin Matthew Park) == | |||
[[File:WIKI-4-2.png|800px]] | |||
Latest revision as of 08:25, 10 May 2019
Propanal (Nora Liu)
A reaction of 1-bromopropane with NaOH and then PCC to form propanal.png)
addition of Grignards to Aldehydes (Tyria Heath)
.png)
Butanal (Hailey / Yingqian Qin)
A reaction of butanol with chromium trioxide and pyridine to form butanal.
Rosenmund Reduction (Abena Afari)
An example of a Rosenmund reduction, where hydrogenation of acyl chlorides gives aldehydes. In this case, 2-naphthoyl chloride is reduced to 2-naphthaldehyde. 
Formation of 2-methoxybenzaldehyde: George Kaslow
Kiliani-Fischer Synthesis (Dong Jin Matthew Park)
