Show the appropriate alkene, reagents and solventd necessary to synthesize the follow alcohols specifically. 1e Name:...
10. Write the name of the reagents needed to synthesize the products specified. Substrate Reagent 1 Reagent 2 Products Intermediate Markovnikov or carbocation anti- 3-center Markovnikov Concerted Oxidative cleavage Zaitzev or Hoffman More substituted alkene Less substituted alkene 2° or 3° alcohols 1° alcohol dialcohols alkane cyclopropanation Carboxylic acid CO2
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...
8.) (10 points) Synthesize the following alcohols from benzene or toluene, and/or small alcohols, using formaldehyde if needed, and any inorganic reagents: он b) 9.) (6 points) Give the characteristic ranges and appearances of the peaks in the IR spectrum for the following functional groups: (a) OH (b) CO (c) C-H
4. Provide the missing information (reagents, solvent, etc.) that is necessary to convert the alkene in the кон он
Shown below on Fischer projections are two enantiomeric alcohols. What alkene and what reagents would yield these alcohols upon reacting with each other? Complete the alkene template below to show the structure of the alkene and provide the required reagent(s) by writing it/them above/below the reaction arrow. CH3 CH3 D -OH HO -D X + H -CH2CH3 H3CH2C- CH3 Н. CH2CH2CH3 CH2CH2CH3
Name Show how you would synthesize the alkene below using Wittig chemistry. Show the full chemical mechanism and all steps. (6 pts.)
Give reagents necessary to synthesize the molecule below using the Stork enamine synthesis. Show all steps in detail.
show the reactants and reagents that would be needed to synthesize this compound from an ether ОН
Show the following (Label reagents, products, reactants, and mechanisms): Reaction of Alkyl halide (geminal) to synthesize alkene oralkyne (note mole equivalence of Nu:) Reaction of Alkyl halide (vicinal) to synthesize alkene or alkyne (note mole equivalence of Nu:)
H D) Suggest a method to efficiently synthesize each of the following molecules from an alkene using the reactions. we have learned so far. Give the starting alkene and all reagents necessary. In order for the synthesis to be efficient, the desired product should be the major product formed Br Н,с, На Нс 1 CH3 сH, он На сH CH3 2 Нас" Reicion P ,Br 3 осн, CHy Br Н,с. Нас