In a table form, use the following compounds: formaldehyde, acetaldehyde, acetone, benzaldehye and acetophenone and write the reagents used in each tests, the probable carbonyl compounds positive to these reagents and the expected results.
In a table form, use the following compounds: formaldehyde, acetaldehyde, acetone, benzaldehye and acetophenone and write...
Starting from benzene, acetone, acetaldehyde, cyclohexene, and methyl halides use common reagents to design syntheses for the following compounds. Any source of carbon in your product must be synthesized from these compounds. 0 7.
Convert acetophenone (C6H5COCH3) into the following compound. You may use any other organic compounds or required inorganic reagents. Draw both reaction intermediates, and select the single best set of reagents for each of the three reactio steps.
Write a stepwise mechanism to illustrate the "crossed aldol condensation" of benzaldehy de and acetaldehyde. (a) How would you distinguish between the following pair by use of 'H NMR? (b) Sketch a possible spectrum for each. acetophenone and ptolualdehyde 1. 2.
Write a stepwise mechanism to illustrate the "crossed aldol condensation" of benzaldehy de and acetaldehyde. (a) How would you distinguish between the following pair by use of 'H NMR? (b) Sketch a possible spectrum for each. acetophenone and p-tolualdehyde 1. 2.
Write a mechanism for the acid-catalyzed reaction of formaldehyde with to form a hydrate. Use curved arrows to show movement of electrons н* н он й нон + H,0 - Hс нон
How would you synthesize the following compounds from botanic acid using reagents from the table? Use letters from the table to list reagents in the order used (first at the left).
4. Draw the open-chain carbonyl compounds and the nucleophiles used to form the following nucleophilic addition products. a.
1. Based on the physical and chemical properties you observed in your unknown and each of the carbonyl compounds, identify your unknown and explain fully (using at least 2 tests) how you came to your conclusion. and you believe it is Your unknown letter is Explain based on the results of at least 2 tests/observations: POST-LAB QUESTIONS: 1. Predict the product of the following reactions. If no reaction occurs write "NR" CH CH CH 2. Which test(s) would you use...
Which of the following atoms would be expected to form negative ions in. bnary lonic compounds & which would be expected to form positive ions ? K, Li, o,V, Rb, cl, Au, I, Bi Expected to form negative ions! Expeeded to form positive ions? 11 Rank in (< the bonds (H-I, C-Br, IF, N-H) order of increasing Plarity using =, or ) 2. 0/0.3 points Previous Answers Predict which of the following compounds are ionic and which are covalent based...
One of the most important uses for Grignard reagents is their addition to carbonyl compounds to give new carbon-carbon bonds. In this reaction, the carbon of the organometallic compound acts as a nucleophile to add to the positive carbon of the carbonyl forming an alkoxide ion intermediate. Aqueous acid is used in the second step to protonate the alkoxide ion and form the product alcohol. Draw the structure of the product(s) of step 1 when the following compound reacts with...