Synthesize the following starting with only alkanes or halo alkanes that have 3 or less carbons....
3) Starting with alkyl halides (alkanes with halogens already on them) of two carbons or less, synthesize the following compounds. c-c-c-c ---- C-C-C-0-C OH OH OH C- C- C
Synthesize using alkanes or alcohols of 3 or less carbons, inorganic reagents, oxidizing or reducing agents. CH2=CHCH2 -C-CHCH3 CH3
Synthesize these specific structures. Be sure to include synthesis and retrosynthesis including synthons. Only carbon source permitted is/are: Pyrrole, Benzene, alkanes with less than or equal to three carbons, carbon dioxide, carbon monoxide, cyanide. -Reagents created in situ must be drawn from their stable ingredients Name each reaction, example of this: F. C. Acetylation or reaction type such as free rad or electrophilic aromatic substitution. CI Synthesize these specific structures. Be sure to include synthesis and retrosynthesis including synthons. Only...
How do you make 3-cyclopentane-1-propanal with starting reactants composed of only 6 carbons or less? I'm confused about how to synthesize the compound. Explanation about why the specific reagents are chosen would be appreciated!
Synthesize the molecule below using any of the following reagents: cyclopentane, alkanes, alkenes, or alcohols of three carbons or less, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. show each intermediate and the reagents needed for each step. E. SYNTHESIS: (15 points) Synthesize the molecule below using any of the following reagents: cyclopentane, alkanes, alkenes, or alcohols of three carbons or less, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. Show each intermediate and...
help with synthesis of these how would I synthesize the end product starting with 3 carbons -- -- e KMA04 wld Heo NGNHA
Show how you would synthesize the following 3- amine in good yield using alcohols of carbons 4 or less as your only source of carbon CH3 、CH3
Show how you could synthesize 3-pentanol starting with molecules of no more than two (2) carbons.
suggest 2 different synthesis methods Using the starting material on the left, synthesize the product on the right. you can only use the starting material and any acyclic compounds with less than 8 carbons Synthesize any c8 acyclic or less
List different two methods of synthesizing propionaldehyde starting only with hydrocarbons with 4 or less carbons.