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Q: Please Write SteP by Step Answer Otherwise I give you DISLIKES !
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Q: please give Step by Step Solution Otherwise i give you DISLIKE !!
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Prepare the compound by using suitable reagents. More than one step will likely be required.
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- (a) Rank the following compounds in order of increasing acidity. (b) Which compound forms the strongest conjugate base?Arrange these compounds in order of increasing boiling point (values in °C are -42, -24, 78, and 118). (a) CH,CH,OH (b) CH,OCH, (c) CH,CH,CH, (d) CH,COOHRank each set of compounds in order of increasing basicity.(a) NaOH, NH3, CH3NH2, Ph¬NH2 (
- When trichloroacetaldehyde is dissolved in water, almost all of it is converted to the hydrate. Chloral hydrate, the product of the reaction, is a sedative that can be lethal. A cocktail laced with it is known—in detective novels, at least—as a “Mickey Finn.” Explain why an aqueous solution of trichloroacetaldehyde is almost all hydrate.19.39 (a) Rank the following compounds in order of increasing acidity. (b) Which compound forms the strongest conjugate base? O₂N. OH A B OH C OH D OH(a) Explain how NaBH, in CH;OH can reduce hemiacetal A to 1,4-butanediol (HOCH,CH,CH,CH,OH). (b) What product is formed when A is treated with Ph;P=CHCH,CH(CH),? (c) The drug isotretinoin is formed by reaction of X and Y. What is the structure of isotretinoin? Although isotretinoin (trade name Accutane or Roaccutane) is used for the treatment of severe acne, it is dispensed under strict controls because it also causes birth defects. PPha NaOCH,CH3 HO- isotretinoin HO A Br X Y
- Illustrate the determining the Relative Acidity of Compounds ?Arrange the following molecules in increasing order of acidity. Base it only on their structural differences and explain how it is so. 1. Butanoic acid, Propionic acid, Propylamine, ButaneArrange the following molecules in increasing order of acidity. Base it only on their structural differences and explain how it is so.