Show how you would use Grignard syntheses to prepare
the following alcohols from the indicated starting materials and
other necessary reagents.
a) octan-3-ol from hexanal, CH3(CH2)4CHO
Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting...
Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting materials and any other necessary reagents. Draw the Grignard reagent and any other organic reagents needed. 11 RUVIUWI Constans i Pendulu Part F Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting materials and any other necessary reagents. Draw the Grignard reagent and any other organic reagents needed. ОН -C-CH CH, from C-OCH.CH Draw the molecules on...
Show how you would accomplish the following synthesis, in good overall yield, using the indicated starting materials and any other necessary reagent(s) (as long as these are involved in reactions presented/reviewed in course notes/lecture videos). State clearly all required reagents and conditions (if these are important for the outcome of the reaction). There is no need to provide mechanistic details or to show retrosynthetic analysis. (Important: please, keep in mind that submission of unnecessary content that is incorrect will be...
Show how you would accomplish the following synthesis, in good overall yield, using the indicated starting materials and any other necessary reagent(s) (as long as these are involved in reactions presented/reviewed in course notes/lecture videos). State clearly all required reagents and conditions (if these are important for the outcome of the reaction). There is no need to provide mechanistic details or to show retrosynthetic analysis. (Important: please, keep in mind that submission of unnecessary content that is incorrect will be...
Show how you would accomplish the following synthesis, in good overall yield, using the indicated starting materials and any other necessary reagent(s) (as long as these are involved in reactions presented/reviewed in course notes/lecture videos). State clearly all required reagents and conditions (if these are important for the outcome of the reaction). There is no need to provide mechanistic details or to show retrosynthetic analysis. (Important: please, keep in mind that submission of unnecessary content that is incorrect will be...
3. Propose reasonable syntheses of each of the following compounds from the given starting materials. You may use any other readily available alkyl halides, solvents and reagents as necessary. More than one step is necessary. Show all intermediates, reactions, reagents and conditions clearly. It is not necessary to show the mechanism. HCECH HCECH , X HCECH HC=CH M H OHC (30 marks)
Can you show the mechanism thank you!!! Devise 2 different syntheses(list the starting materials and any reagents) of 3-methyl-3-pentanol. Each syntheses must involve a Grignard reagent.
3. (15 pts.) Provide retro- and forward syntheses of the following compound from the indicated starting materials. Show all reagents required for each transformation. Individual amino acids NCO2H NH2 H21
II. What carbonyl compounds and Grignard reagents would you use to make the alcohols shown below? Show all possibilities. No mechanism necessary. (8 pts) НО. b OH
Question 3 Show how you can synthesize the following compounds using the indicated starting materials and any other necessary substances or reagents. (20 pts) A. CH COOH (starting from ortho-nitrotoluene) B. HN (starting from nitrobenzene)
Use Dieckman cyclization to prepare the following compound from the indicated starting material. You may use any organic and inorganic reagents necessary. Your answer should clearly show your synthetic scheme complete with reagents and products for each step.