Answer:
123456789dfghjk
Explanation:
gggyyhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhnnnnnnnnnnnnnnnnvvvvvvvvvvvvccccccccccccccxxxxxxxxxxzzszsdfvbhngyfdd
Answer:
Reduction of Aldehydes and Ketones. Hydride reacts with the carbonyl group, C=O, in aldehydes or ketones to give alcohols. ... Reduction of ketones gives secondary alcohols. The acidic work-up converts an intermediate metal alkoxide salt into the desired alcohol via a simple acid base reaction.
The carbon atom of a carboxyl group is in a relatively high oxidation state. Diborane, B2H6, reduces the carboxyl group in a similar fashion. ... Sodium borohydride, NaBH4, does not reduce carboxylic acids; however, hydrogen gas is liberated and salts of the acid are formed.
Primary alcohols can be oxidized to form aldehydes and carboxylic acids; secondary alcohols can be oxidized to give ketones. Tertiary alcohols, in contrast, cannot be oxidized without breaking the molecule's C–C bonds.
A secondary alcohol can be oxidised into a ketone using acidified potassium dichromate and heating under reflux. The orange-red dichromate ion, Cr2O72−, is reduced to the green Cr3+ ion. This reaction was once used in an alcohol breath test.
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65 Grams is the mass of the beaker because you just take the mass of Water + Beaker and take the water away now you have the mass of the beaker
<u>The Ingredients required are...
</u>GBL (gamma-butyrolactone)
BD (butanediol)
GBL is an ingredient used when stripping paint
BD is an ingredient used in making plastics or adhesives
This drug is illegal because no one can detect it in a drink when dissolved in
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