How could you use HNMR to tell if your final product (2-(2,3-dimethyloxybenzylinene)indan-1-one) was contaminated with unreacted 1-indanone?
How could you use HNMR to tell if your final product (2-(2,3-dimethyloxybenzylinene)indan-1-one) was contaminated with unreacted...
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.
Crossed aldol condensation of 3.4-dimethoxybenzaldehyde and l-indanone your co m ments cholateOH -4.0 dehydration formation OH O CHOY carbonyl addition initial aldol product...
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
How can you tell if your grain product is a whole-grain product? Select one grain product (from your kitchen, grocery store, or internet) package to answer the questions below. What is the name of your food? Add a picture of the foods ingredient list - not the food label. Based on what you see in the ingredient list would you say that your grain product is a whole-grain? Why or why not?
Product was formed successfully based on the exp. below (about
85% yield), please interpret/discuss HNMR/IR in as much detail as
possible and assign peaks on HNMR (which peak represents which
protons of which group, etc). Note: I already know how you
determine the formation of the product so you can skip that part of
part b).
Based on this exp:
Discuss the IR spectrum and what is the peak in IR that you can see for a specific functional group...
If you suspect your product is contaminated with n-butyl alcohol and not acetic acid, what spectroscopic technique would you use to confirm it.
Can you explain how the J values on HNMR support an E or Z configuration as it relates to the reaction of 2,3-dibromo-3-phenylpropanoic acid with acetone as the solvent, then with water as the solvent, to yield Beta-Bromostyrene. J values for Acetone give a ratio of 1:2 98%-cis 2%-trans. For Water it's 1:4 20%-cis, 80%-trans. Thank you.
You work for a factory making bricks. A coworker accidentally contaminated one of the bricks with lightweight material and it must be removed. Given a pile of 50 bricks and a balance scale, how can you find the one that weighs less? The scale can hold any number of bricks on each side of the scale at one time, and it will tell you if the two sides weigh the same, or which side is lighter if they do not...
Tell how you could use recentering and rescaling to simplify the computation of the mean and standard deviation for this list of numbers: 5478.1 5478..3 5478.3 5478.9 5478.4 5478.2
Explain how you could use gas chromatography to determine amounts of o-nitroanisole and p-nitroanisole in final product.
Tell us of a problem with a product which bothers you. How would you use technology to solve the problem? - Propose more than one potential solution (max 3) Compare and choose the best solution for the problem How would you measure whether the chosen solution is working? What might be the reason for this chosen solution to fail ?