. conclusions from permanganate test. Based on observations, comment on positive and negative tests with reasoning (no reactions necessary) . First, recalculate the theoretical yield using the actual mass of oleic acid you used. Note: The percent yield of a reaction is always calculated as (mass of pure product/theoretical yield) *100. As you were not required to purify it, you may just present this as a "yield of crude product" calculation. IV. Summary Question For the reaction below, suggest any three possible structures of alkene reactants that could be used to make the product shown using a hydrogenation reaction. ? NH, HCOẶ Pd/C, CH₂OH

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conclusions from permanganate test. Based on observations, comment on positive and negative tests with reasoning (no reactions necessary)
First, recalculate the theoretical yield using the actual mass of oleic acid you used. Note: The percent yield of a reaction is always calculated as (mass of pure
product/theoretical yield) *100. As you were not required to purify it, you may just present this as a "yield of crude product" calculation.
IV. Summary Question
For the reaction below, suggest any three possible structures of alkene reactants that could be used to make the product shown using a hydrogenation reaction.
?
NH, HCO;
Pd/C, CH₂OH
Choose a submission type
Transcribed Image Text:. ● conclusions from permanganate test. Based on observations, comment on positive and negative tests with reasoning (no reactions necessary) First, recalculate the theoretical yield using the actual mass of oleic acid you used. Note: The percent yield of a reaction is always calculated as (mass of pure product/theoretical yield) *100. As you were not required to purify it, you may just present this as a "yield of crude product" calculation. IV. Summary Question For the reaction below, suggest any three possible structures of alkene reactants that could be used to make the product shown using a hydrogenation reaction. ? NH, HCO; Pd/C, CH₂OH Choose a submission type
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