provide the mechanis for this reaction and suggest a protocol on how can i prepare 1g...
how
can i synthesize 1g of that product in a laboratory using
hypervalent Iodine chemistry? please show the full protocol and
provide chemical conditions
Scheme 1 ??? Meo ome Scenario #1:
can
you please provide the nane of the product
i
mean the chemical name*
also how to prepare the product using hypervalent iodine
Scheme 1 OH ???, Мео оме
1. Provide the missing conditions for both steps and show how the amide can be converted to the corresponding acid chloride. Step 1 Step 2 Step 1 Conditions for step 1 (brain-twister: is there just one way?): Conditions for step 2 (same brain-twister): Full reaction scheme: 2. Consider the following reaction: 1. NaOM/MeOH 2. H,0* Does it have a specific name? How many products are possible? Show all of them. Suggest a synthetic route that leads to a lesser number...
7. Suggest how you would synthesize the compound X shown below. Make sure that compound X is the ONLY product possible! Question 7 and 8 Hint (Remember for the exam!): To answer this question, you simply need to provide the structures of the organic substrate and a reagent (in this specific case, an alkyl halide and a base or a nucleophilie and electrophile) that can be used to obtain the product X shown by using a correctly designed reaction (an...
Helpppp
Your cells are ready to split and you prepare to scale-up. Write a protocol for this scale-up in enough detail that anyone in your laboratory could follow your exact procedure. Your protocol should answer the following questions. How will you release the cells from the substrate? How will you split the contents of the flask (what kind of flasks, how many flasks, how much medium, etc.) for scale-up (10 points)? All of your flasks of cells are ready to...
How can I prepare Propyl Benzhydryl Ether using William ether synthesis? I have to use diphenylmethanol as a starting material. Please provide me the whole procedure with the appropriate steps and amount of substances I need to use. Thanks!!
Provide the reagents necessary to complete the following
transformations, which can be accomplished in three steps or
less.
the
concepts are: Carbonyl Compounds/acidity, Enol/Enolate,
Aldol reaction(Self/Crossed/Intra), Claisen
Condensation(Intra/Crossed/Hydrolysis/Decarboxylation of beta
keto-esters), reagent RuBisCO, and Alkylation of Enolate
Ions. Please help with answers within these concepts.
Thank you.
the concepts are: Carbonyl Compounds/acidity,
Enol/Enolate, Aldol reaction(Self/Crossed/Intra), Claisen
Condensation(Intra/Crossed/Hydrolysis/Decarboxylation of beta
keto-esters), reagent RuBisCO, and Alkylation of Enolate
Ions. Please help with answers within these concepts.
Thank you.
1. Prrovide the reagents...
1. Provide the missing conditions for both steps and show how the amide can be converted to the corresponding acid chloride Step 1 Step 2 Conditions for step 1 (brain-twister: is there just one way?): Conditions for step 2 (same brain-twister): Full reaction scheme:
1. Provide the missing conditions for both steps and show how the amide can be converted to the corresponding acid chloride. Step 1 Step 2 Conditions for step 1 (brain-twister: is there just one way?): Conditions for step 2 (same brain-twister): Full reaction scheme:
can you show me how each reagent affects the starting material
, I undertand that the NaCN,DMF adds the CN where the br is at but
dont understand what the H2so4 ,h20 does
Meo Meo YB 1) NaCN, DMF 2) H2SO4, H2O, A. Meo ОMe