Starting with appropriate unlabeled organic compounds, show syntheses of each of the following: Your answer is incorrect. (a) Draw the reagents needed to produce C6H5-C=C-T. Draw Your Solution
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- How could you convert each of the following compounds into butanoic acid? Write each step showing all reagents. (a) 1-Butanol (b) 1-Bromobutane (c) 1-ButeneStarting with appropriate unlabeled organic compounds, show syntheses of each of the following: (a) Draw the reagents needed to produce C6H5-C=C-T. Draw Your SolutionNaH HO HO PBR3 A (a) Name the functional groups in compounds A and B, including, if relevant, whether they are primary (1°), secondary (2°) or tertiary (3'). (b) Propose a reagent that could be used to convert A into B. (c) Draw the structure of the intermediate C formed by reaction of compound A with NaH. (d) Propose the structure of the organic compound D formed by reaction with PB.3. (e) Could HBr be used for the conversion of A into D? Explain very briefly.
- How could you convert butanoic acid into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) 1-Bromobutane (c) 1-ButeneHO CH30 Na A + B O,N pK =7 (a) Provide structures for A and B (including nonbonding electron pairs and formal charges where necessary), where A is the conjugate acid and B is the conjugate base of the reaction. Answer: (b) Provide and arrow pushing mechanism to show how A and B are formed. Answer: (c) Will the reaction proceed from left to right (i.e. are A and B favoured at equilibrium)? Explain your answer. Answer: (d) Draw all important resonance contributors of the conjugate base B. Rank the contributors from most stable to least stable (if contributors are equally stable indicate this with an equals sign)Please answer all subparts, a,b,c, and d. And only part a should have a major and minor product.
- Determine the major product of the reaction shown in the box د b C A B C NaBH CH₂OH Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. d D OH OH B ON OH C b DPlease answer parts a,b,cGive the major product(s) of the following reaction. 1) NaCN 2) H+
- How could you convert butanenitrile into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) ButylamineGive reasons for the following: (i) p-nitrophenol is more acidic than p-methylphenol. (ii) Bond length of C—O bond in phenol is shorter than that in methanol. (iii) (CH3)3C—Br on reaction with sodium methoxide (Na+ _OCH3) gives alkene as the main product and not an ether.b) Refer to the following equation to answer Q3b (i), (ii) and (iii). CH3 H,SO, Н—с—он C-CH3 ? + H2O Но- ČH3 (i) Determine the product of the above reaction. (ii) Name the above reaction. (iii) Propose the mechanism for the above reaction.