Show reagents and experimental conditions you might use to convert 3-methyl-1-pentyne into each of the following. Please show and explain all steps!
Show reagents and experimental conditions you might use to convert 3-methyl-1-pentyne into each of the following....
8. Name the following: CH2 CH3 a) 1-hexyne b) 2-ethynylbutane c 3-methyl-1-pentyne methyl-4-pentyne 4-methyl-5-pentyne
_________________________________________________________________________________________________________________________________ d. Prepare octane from 1-pentyne, indicate each needed reagents. e. Synthesize cis-2-hexene from 1-pentyne and an alkyl halide. f. Synthesize trans-2-hexene from 1-pentyne and an alkyl halide. Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. a.
Name the following compound CECH CH,CH2CHCHs O 3-ethyl-1-butyne 3-methyl-1-pentyne O 3-methyl-4-pentyne O 2-ethynebutane O 1-hexyne
Name the following: СН2СН3 | CH3-C-CEC-H H A. 3-methyl-1-pentyne B. 2-ethyl-3-butyne OC. 1-hexyne OD.3-methyl-4-pentyne E. 2-ethynyl butane
Design a synthesis of 4-methyl-2-pentyne from 3-methyl-1-butene. H2C Part 1 out of S Choose the best option for the immediate precursor to the target molecule. H3C HI A Br Br Br H Br E H,C- H 3 attempts left Check my work Click the "draw structure" button to launch the drawing utility. Give the structure corresponding to 4-tert-butyl-5-decyne. draw structure Be sure to answer all parts. Give the IUPAC name for the following compound. (select) (select) Be sure to answer...
Question: What reagents are used in the following: 1) Reduction of methyl pent-3-enoate to pentan-1-ol (two steps) 2) Oxidation of 3-methylbut-1-ene to 3-methyl-2-oxobutanoic acid (two steps) 3) Oxidation of 2-bromobutane to butyraldehyde (three steps) I was able to draw these out with the steps but cannot decide which reagents are applicable, especially for the breakdown of double bonds. Please help! Thank you!
Starting with acetylene use a sequence of reagents to show how you could make each of the following products. Note that some steps will be redundant so please just start from a common intermediate once you have shown its synthesis. For example, all of the other products can be made from either 1-butyne or 2-hexyne. You may not use any other source of C other than methyl bromide, calcium carbide, chloroform and the products you can make from these sources....
Show how the following compound could be prepared from 1-butyne. You may use any necessary reagents. You must show all stable intermediates formed along the way and all necessary reagents used (20 points). multiple steps! Br
Starting with acetylene use a sequence of reagents to show how you could make each of the following products. Note that some steps will be redundant so please just start from a common intermediate once you have shown its synthesis. For example, all of the other products can be made from either 1-butyne or 2-hexyne. You may not use any other source of C other than methyl bromide, calcium carbide, chloroform and the products you can make from these sources....
8.69 Identify the reagents you would use to achieve each of the following transformations: (a) Convert tert-butyl bromide into a primary alkyl halide (b) Convert 2-bromopropane into 1-bromopropane