Acetals as protecting groups and thioacetals | Organic chemistry | Khan Academy

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Khan Academy Organic Chemistry

Khan Academy Organic Chemistry

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How acetals are used as protecting groups. Thioacetals are similar to acetals, but form from reaction of an aldehyde with a thiol (not an alcohol). Created by Jay.
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Organic Chemistry on Khan Academy: Carbon can form covalent bonds with itself and other elements to create a mind-boggling array of structures. In organic chemistry, we will learn about the reactions chemists use to synthesize crazy carbon based structures, as well as the analytical methods to characterize them. We will also think about how those reactions are occurring on a molecular level with reaction mechanisms. Simply put, organic chemistry is like building with molecular Legos. Let's make some beautiful organic molecules!
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Пікірлер: 7
@shotdoctor5869
@shotdoctor5869 6 жыл бұрын
Why does the carboxylic acid not react with the alcohols the way the ketone does?
@vijayvyas5075
@vijayvyas5075 5 жыл бұрын
TheShot Doctorr did u get an answer to this? i too have the same doubt. please share if u know.
@briggshightower2609
@briggshightower2609 7 жыл бұрын
Why make the video when hardly any arrow pushing is shown. We get tested on those kinds of things and it gives reason to the synthesis
@izkl5769
@izkl5769 3 жыл бұрын
it helpss a lot, thank you!
@lionelwitherspoon5410
@lionelwitherspoon5410 7 жыл бұрын
Missed the hemiketals actual step.
@GreenMarble
@GreenMarble 8 жыл бұрын
Will Raney Ni do the same thing with acetal protecting groups?
@waldmannfisch6970
@waldmannfisch6970 7 жыл бұрын
no, raney nickel will do nothing to acetals
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