Using phenol, dimethyl sulfate, and NaOH, show how you would synthesize methyl phenyl ether.
The anisole (phenyl methyl ether) can be synthesised by using the given reagent and the formation mechanism is shown in following picture,
Using phenol, dimethyl sulfate, and NaOH, show how you would synthesize methyl phenyl ether.
How to synthesize 2-methyl-1-phenyl-1-propanol
Use retrosynthetic analysis to suggest two paths to synthesize 2-methyl-1phenyl- 1-propanol using the Grignard reaction. (Click and drag the appropriate image to the correct position in the following reactions.)
Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions: Reactions 1. Halogenation 2. Nitration 3. Sulfonation 4. Friedel-Crafts acylation 5. Friedel-Crafts alkylation 6. Oxidation of methyl group 7. Reduction of nitro group • Choose the starting material from the drop-down list • Enter the number(s) of the desired reactions in the order that you wish to use them without commas between • If a reaction is used more than once, enter its number...
Propose a mechanism to synthesize tert-butyl methyl ether using tert-butyl alcohol and methyl alcohol. You can include any other inorganic reagents needed, and avoid using undesirable ones. Please use specific examples and explain, I want to understand how to do this.
Use retrosynthetic analysis to suggest two paths to synthesize 2-methyl-1-phenyl-1-propanol using the Grignard reaction.
Use retrosynthetic analysis to suggest a way to synthesize
2-methyl-1-phenyl-1-butanol using the Grignard reaction. (Click and
drag the appropriate images to the reactant positions in the
following reaction.)
5. (10 pts.) How would you synthesize o-chlorophenol (B) from phenol (A) without obtaining undesired multi-chlorinated phenols Show a reasonable synthetic route with reagents h mechanisms required) ic r Cl но HO
5. (10 pts.) How would you synthesize o-chlorophenol (B) from phenol (A) without obtaining undesired multi-chlorinated phenols Show a reasonable synthetic route with reagents h mechanisms required) ic r Cl но HO
How would you prepare benzyl methyl ether using a Williamson ether synthesis? The list of reagents to choose from are: 2-Chloro-norborane, Benzyl chloride, 2-Chloro-2-methylpropane, 4-Chloro-1-butanol, and Chlorobutane. I was reading online and it kept mentioning SN2 reactions, using an alcohol, and an alkyl halide for the synthesis. My guess would be using Benzyl Chloride and another one with an OH attached, but I could be completely wrong. Please help and explain by showing the reaction mechanism. Thank you so much!...
Show how you would synthesize the following acid using carbonation of a Grignard reagent. Show how you would synthesize the following acid using carbonation of a Grignard reagent.
10) Show how to synthesize 4-Phenyl-2-butanone using the Acetoacetic Ester Synthesis. Start with Ethyl 3-oxobutanoate (C6H1003).
17-52 Show how you would synthesize the following compounds, starting with benzene or toluene and any necessary acyclic reagents. Assume para is the major product (and separable from ortho) in ortho, para mixtures. 1-phenyl-1-bromobutane 1-phenyl-1-methoxybutane 3-phenylpropan-1-ol ethoxybenzene 1,2-dichloro-4-nitrobenzene 1-phenylpropan-2-ol p-aminobenzoic acid 2-methyl-1-phenylbutan-2-ol 5-chloro-2-methylaniline 3-nitro-4-bromobenzoic acid 3-nitro-5-bromobenzoic acid 4-butylphenol 2-(4-methylphenyl)butan-2-ol