the top half of the image depicts the synthesis of
2-[(3,4-dimethoxyphenyl)methylene]-2,3-dihydro-1H-inden-1-one from
1-indanone and 3,4-dimethoxybenzaldehyde. The bottom half of the
image attached shows the table of chemicals used in the reaction.
How would I calculate theoretical yield and furthermore, the
percent yield? This experiment had a lot of chemicals used and I
don't know where to start.To find out the percent yield, first we will calculate the number of moles used in the reaction to determine limiting reagent in the reaction.
Number of moles of 1-indanone = 0.20/132.16 = 0.0015 moles
Number of moles of 3,4-dimethoxy benzaldehyde = 0.25/166.17 = 0.0015
Both the reactant are in 1:1 ratio and we can take any of the molecule for the calculation of percent yield (the limiting reactant should be taken for percent yield calculation)
Therefore, 166.17 gm of 3,4-dimethoxy benzaldehyde gives 280.3 gm of product
Then, 0.25 gm of 3,4-dimethoxy benzaldehyde will give x gm of product
Amount of product expected (theoretical yield) = (0.25*280.3)/166.17 = 0.42 gm
Amount of product obtained in the reaction = 0.171 gm
Percent yield of reaction = (0.171/0.42)*100 = 40.71%
the top half of the image depicts the synthesis of 2-[(3,4-dimethoxyphenyl)methylene]-2,3-dihydro-1H-inden-1-one from 1-indanone and 3,4-dimethoxybenzaldehyde. The...
Provide a stepwise mechanism for the formation of
2-[(3,4-dimethoxyphenyl)methylene]-2,3-dihydro-1H-inden-1-one from
3,4-dimethoxybenzaldehyde and 1-indanone. Please show all steps!
This is a crossed aldol condensation. Thanks!
Crossed aldol condensation of 3,4-dimethoxybenzaldehyde and l-indanone CHO CH,0 NaOH spolu co m ments CH,O CH,09 enolate formation OH -H,0 T dehydration CHO OH O CH,0 CHOA carbonyl addition CH,0 initial aldol product