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4..Provide an alternate synthesis to synthesize each of the products 1-phenyl-1-propanol and 2-phenyl-2-propanol.
EXPLAIN IN DETAIL WHY******
Already used: benzaldehyde and ethylmagnesium bromide for 1-phenyl-propanol and acetone with phenylmagnesium bromide for 2-phenyl-2-propanol.
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- a. What reagent(s) are needed to synthesize the enamine below. Also, draw the resonance structure(s) for the enamine. b. Predict the product of the reaction between the enamine from part a and ethyl iodide. Also explain why it forms, including any selectivities. Hint: Consider the type of reaction alkyl halides take part in and the resonance structure(s) in part a. EtlInstructions. Briefly describe the following given reactions. 2. The conversion of benzaldehyde into benzophenone. HNO, SOCL, (Oxidation) Benzaldehyde (Friedel-Craft acylation) Anhyd. AICI, Benzophenone AN SWERS: DeskWhich or which of the statements given below is correct. I) Maleic anhydride is a carboxylic acid derivative and its reaction with water is a reduction reaction. II) Fumaric acid and maleic acid are stereoisomers of each other III) Since fumaric acid has a more stable structure than maleic acid, its boiling point is higher. A. Solo I B. I and III C. II and III D. I, II, III E. Solo III
- ****** 3. Provide a synthesis scheme of 2-methylbutanoic acid starting with a malonic ester and any necessary reagents.Synthesize Chloramphenicol from Toluene or Benzaldehyde. Draw and explain step by step please.(p.s: if you can, can you write what the reagents does?) (Drug Chemistry)Provide IUPAC of the starting material for the reaction shown below. Choose ALL that apply BB IUPAC of starting material Multiple answers: Multiple answers are accepted for this question Select one or more answers and submit. For keyboard navigation... SHOW MORE a S-ethyl-2-mmhyloctanoic acid b 5-ethyl-2-methyl-1-octanol C 5-ethyl-2-methyloctanal d S-ethyl-2-methyloctanone RC9.4 Homework Unanswered Due Today, 8:00 PM H₂Cro₁ H₂SO4 (aq) Provide IUPAC name for the final product in the reaction below OH 1. LIAIH 2. H₂O je IUPAC of final product OH
- Wittig reactions with the following -chloroethers can be used for the synthesis of aldehydes and ketones. (a) Draw the structure of the triphenylphosphonium salt and Wittig reagent formed from each chloroether. (b) Draw the structural formula of the product formed by treating each Wittig reagent with cyclopentanone. Note that the functional group is an enol ether or, alternatively, a vinyl ether. (c) Draw the structural formula of the product formed on acid-catalyzed hydrolysis of each enol ether from part (b).A certain compound is known to contain an aromatic benzene ring but failed to produce a fragrant yellow solution upon subjecting it to the nitration test. What may be a possible explanation for this? A. The benzene ring is part of a highly conjugated, blue dye molecule. B. The benzene ring contains a strong electron-withdrawing group. C. The benzene ring has no available sites left for electrophilic attack. D. All of the given. Kindly explain your answer in detail.Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C. ... NH2 HCI/H₂O reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one. + 4 n [ ?
- 4) a) Attempting to alkylate t-Butylchloride with the enolate of acetone gives an undesired product. Draw the structure of the product and explain why it forms. b) [self-study not grade: Compare the difference between the alkylation of ketones and the alkylation with malonic ester or acetoacetic ester. Provide a reason for to explain why aldehydes are rarely used in this kind of alkylation reaction. ]NB: All bonds to benzene must be made using Electrophilic Aromatic Substitution (including Friedel-Crafts reactions) or Nucleophilic Aromatic Substitution! Design a synthesis of each of the following target molecules, starting with benzene: a. pentylbenzene b. 2-chloro-1-propyl benzene d. 3-chloro-1-propyl benzene d. 1-phenyl-1-butanolKindly answer the following questions below. You may use illustration to help explain your answer a. Illustrate and explain the difference between Markovnikov and Anti-Markovnikov addition of HBr to alkene. b. Explain why catalytic hydrogenation of alkene proceeds via syn addition c. Explain, using resonance structures, why an OH group of phenol is an ortho/para director.