Show the steps for synthesis of Dimethylamine, labeling each step with the name of the reaction or reaction type and the reagents used. The only starting carbon sources you can use are alkanes with 3 or fewer carbons, CO2, CN-, and CO. Thanks!
Show the steps for synthesis of Dimethylamine, labeling each step with the name of the reaction or reaction type and the reagents used. The only starting carbon sources you can use are alkanes with 3...
**SYNTHESIS QUESTION: HELP NEEDED!** Show the steps for the reagents for the following molecule (Lexapro). I've figured out the synthesis for the molecule on the right(in materials), but I can't figure out how to create the other benzene-based molecule with the nitrile attached that I need to finish the whole molecule. I think that benzaldehyde needs to be synthesized and then converted to an ester and then attached, but I can't figure out how starting from benzene. Please show the...
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...
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...
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
Please explain the mechanisms! 1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Multiple steps are required. The number of steps you use does not matter. Reactions should give the desired product as a major product. For full credit show the product of each step (reaction). If you make use of organometallic reagents such as Grignard, Wittig, organolithium, organosodium, organocopper, etc. you must...
Devise a synthesis of (Z)-3-octene using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps Starting materials нсисынсно-си нос-сцен нос-cң соң,он нонс Reagents + NaNH / NH diodo ethane 1-bromo-3-methybutane H undar catalyst + NaOH HẠO e 1-bromopropane butyl bromide күн clodomethane 1 2-bromopropane H/Pd on carbon I N/NH0 Starting material Reagent for step 1...
Show your steps and reaction conditions clearly. No reaction mechanisms are required. (a) Using acetone and 2.2-dimethylpropanal as your only sources of carbon atoms, show how you would synthesize compound 1. Hint: Reaction of a diol and a carbonyl compound. Starting from 1-ethoxynaphthalene and 3-methylbutanoic acid as your only sources of carbon atoms, show how you would synthesize the ester 1. Hint oxidation of a ketone to ester (C) Suggest a synthesis for compound 1 using as starting materials/reactants benzaldehye....
4) (2 pts each) Outline a synthesis (i.e., simply show the reagents/reactants for the necessary reactions) for each compound below from the designated starting material. Use reagents you've learned about in Orgo I and II. The number of arrows does not necessarily correspond to the number of steps required. As a general rule, any carbon units in the products that were not in the starting materials should come from molecules containing 7 or fewer carbons. Things that don't end up...
Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3 Cl CH3 Alcohol Starting Materials 1. methanol 2. ethanol 3.1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LiAlH4 f. PBr k. CH3 CH2CH2 then H3O L CsHsMgBr (phenylmagnesium bromide); then H3o m. (CHs)2CHMgBr: then Hgo d. HBr i. CH, MgBr, then Ho .Dess-Martin periodinane (DMP) e....
the steps are B,D,H,I,G,D,F,D,C Synthesis You need synthesize cyclopentanone starting with the lactone shown below in 9 steps where 3 of the steps are acid workups. Cheat DH,O (aqueous acid) E pcc F NaOH, heat G NaOCHCH H Na,Cr,0,.aq acid HOCH,CH,, acid, heat NBS Note- there are 3 reagents on this table that are not used - ALL OTHERS ARE USEI Steps Reaction names Give the name of the type of reaction for each step, (examples: acidification, reduction, saponification decarboxylation,...