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6 Cards in this Set
- Front
- Back
What is the systematic name for melonal |
2, 6 - dimethylhept-5-enal |
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A pratical measure to maximise the yield of melonal |
Distill off to prevent further oxidation. So carboxylic acid doesn't form |
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D |
D |
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Would you expect this molecule to rotate in plane polarized light |
No the molecule is planar, so can be attacked from both sides. The racemic gives equal amounts of each isomer |
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State and explain how you would quench the reaction of iodine with propanone |
Add excess sodium hydrogen carbonate, to remove acid |
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Propanoic acid and methanol react to form an ester, name the ester |
Methyl proponate |
