Please give a proper method to synthesize each of the compounds in the image provided. You may only use: ethyl acetate, acetone, benzaldehyde, or benzyl bromide as organic components. You may also use any base of your choosing.
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Please give a proper method to synthesize each of the compounds in the image provided. You...
3. Using only ethyl acetate, acetone, benzaldehyde, or benzyl bromide as organic components, and using any bases you desire, indicate a method to synthesize the following compounds. b. a. i d. C.
1. Write a structural formula for each of the following compounds: (36 pts) (a) m-chlorobenzoyl chloride (b) N-ethyl benzamide (c) dibenzalacetone (d) ethyl acetoacetate (e) 2-ethyl-1-butanamine (t) dibenzylamine 2. Write a structural formula for the principal organic product or products of each of the following reactions: (36 pts) (a) propanoyl chloride and sodium propanoate (b) acetic anhydride and 3-pentanol (c) acetaldehyde and sodium ethoxide (CH3CH2ONa) in ethanol solvent (d) cyclohexanone, benzaldehyde, and NaOH (e) 2-aminopropane and acetyl chloride in pyridine...
42 Show how you mmgnt synthesize each of the following compounds starting with either benzyl bromide or allyl bromide: GEN CN (c) CoH GaHs OMe (d) CaH (e) (f)
can you solve everything please Short Answer 7. Show how you could synthesize these compounds from any compound having three carbons or fewer. You can use any regent necessary, but keep to the three carbons. Сн, снен, с-н снен, сн, ск, сн, сн, 8. Give an example of a synthesis that requires the protection of an ketone. You may use any reaction, any organic compounds. You must show the reaction that does the protecting. 9. Give an example of a...
02. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) (you can also use any one C reagent)
Q2. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) Do (you can also use any one C reagent) ОН (you can also use any two carbon reagent)
Answer all questions please. Not due until April 3rd. -------------------------------------------------------------------------------- Question 1 Not yet answered Points out of 3.00 Consider two compounds shown below. For each compound identify which group is the most acidic, the least acidic, or has mid acidity value (pKa value) он он 1 HO 0H3 Flag question NH3 OH 2 group 1 Choose... group 2 Choose group 3 Chse... group I group IIChoose group III Choose... Choose. Question 2 Not yet answered Points out of 3.00...
Please answer and number each 1. Write a structural formula for each of the following compounds. a) 1-chloro 2,4-dinitrobenzene b (E)-1-phenyl-1-butene c 4-aminobenzoic acid d) 3-ethyl-2-methylaniline e) 2,4,6-trinitrotoluene 2. Give the structure of the major product formed on the following reactions a) sodium ethoxide and benzyl bromide b) 2-phenylpropene and hydrogen chloride CH2CH, CCI4 c) 02N
Complete the following syntheses (you must use BOTH compounds provided). You must synthesize the compound on the RIGHT (ie, the compound the arrow is pointing toward) from the compound on the LEFT. You must use the compounds on the left as your starting material, but you are free to use any other reagents as needed.
Show how you would synthesize the following compound starting with acetylene and compounds containing no more than two carbon atoms as organic starting material. You may use any additional reagents you need Br H H Br