that is hexene not hexane. we are using trans means there must be double bond. so hexene.
7. Using any reagents necessary, provide a synthesis for (2R,3S)-2,3-diethyloxirane starting from 3-hexene, trans-3-hexane/ (2R,35)-2,3-diethyloxirane
Propose a synthesis to produce (2R,3S)-2,3-dibromobutane from acetylene. You can use any inorganic reagents you'd like. You don't have to draw the mechanism - only provide the reagents needed for each step of your proposed synthesis. Br ??? HEH Br exclusive product
This question is worth 10 points. Propose a synthesis to produce (2R,3S)-2,3-dibromobutane from acetylene. You can use any inorganic reagents you'd like. You don't have to draw the mechanism - only provide the reagents needed for each step of your proposed synthesis. Br ??? HH Br exclusive product
show all steps of these synthesis problems (2S,3S)-2,3-hexanediol (a diol has two -OH groups) (33) acetylene Br + En (35) (2R,3S)-2,3-hexanediol (a diol has two -OH groups) (36) Br Он (37) + En он Cl (39) (40) (2S,3S)-2,3-hexanediol (a diol has two -OH groups) (33) acetylene Br + En (35) (2R,3S)-2,3-hexanediol (a diol has two -OH groups) (36) Br Он (37) + En он Cl (39) (40)
Gradescope #4 This question is worth 10 points. Propose a synthesis to produce (2R,3S)-2,3-dibromobutane from acetylene. You can use any inorganic reagents you'd like. You don't have to draw the mechanism - only provide the reagents needed for each step of your proposed synthesis. Br ??? HEH Br exclusive product
6. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 7. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 8. Starting with benene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there...
Devise a synthesis of these compounds starting with 3-carbon alkyl halides. Show any necessary reagents and reaction conditions. All carbons must ultimately come from the 3-carbon alkyl halides. Once you have made a new compound, you may reuse it without making it again. a) Propanone b) Butanoic acid c) 3-hexene
choose the sequence of reagents that provides the most efficient synthesis of 1,2-dicholorobutane starting from butane and using any reagents necessary.24.1 (3).png24.1 (2).png
Provide a reasonable multistep synthesis of the following molecule from the indicated starting material, using any reagents necessary. (Please include the product and reagents of each individual step in your synthesis. DER
Starting with Benzene and using any other necessary reagents of your choice a synthesis for the following compound. Assume that ortho and para isomers can be There may be more than one plausible answer.
Starting from benzene and using any other necessary reagents of your choice, design a synthesis for each of the following compounds. Some problems have more than one plausible 1. answer (g)* in this example, what can be done to minimise the amount of the meta/para isomes. NO2 (h) रेर Br (i) Н-N. Br NH2 (k) Br "SoH