Which of the following ethers can be synthesized by two different Williamson ether syntheses (reaction of an alkoxide anion with an electrophile in an SN2 process? Why ? OR OR OR О D D D
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Q: Please give the following structures IUPAC names, provided with an explanation
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Q: 7) Identify the reagents of product required. Add any Side products not shown. C127 AICI b) AICI3…
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Q: Consider the reaction of a 20.0 mL of 0.220 M C H NHCI (Ka = 5.9 x 10°) with 12.0 mL of 0.237 M…
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- What is the major product of the following ozonolysis reaction? and and HOThe ether molecule below can be prepared in two different ways. Which method is a better way to prepare thedesired product and why?Name and Draw the Phenolof all possible chemical (Electrophilic aromatic substitution) reactions of the compound namely; Halogenation (Chlorination or Bromination) Nitration
- Melamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation fatr this reactivity.Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict themajor products of the reactions of naphthalene with the following reagents. f) fuming sulfuric acidWhat is the major alkene formed when A is treated with POCl3 andpyridine? Explain why the major product is different in these reactions.
- Ethers are generally unreactive, but epoxides react with a variety of nucleophiles. Explainthe reactivity of epoxides in terms of their structure.Choose which compound is more reactive when reacted with N2OH in water solvent and he reason clearly. vs OH HO,QUESTION 7 Which of following statement is incorrect regarding aromatic electrophilic substitution reaction? EAS reaction goes through a carbocation intermediate The rate determining step is loss of proton to form the product Benzene acts as a nucleophile in the EAS reaction Bromine acts as a electrophile in the EAS reaction