Chapter 17: Q28P (page 883)
What substituted alkene would you use in the Heck reaction to make the following products?
Short Answer
⦁ The substituted alkene used in the first reaction is
⦁ The substituted alkene used in the second reaction is
Chapter 17: Q28P (page 883)
What substituted alkene would you use in the Heck reaction to make the following products?
⦁ The substituted alkene used in the first reaction is
⦁ The substituted alkene used in the second reaction is
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Get started for freePropose a mechanism for the bromination of ethyl benzene shown above.
Predict the major products of treating the following compounds with hot, concentrated potassium permanganate, followed by acidification with dilute HCl.
(a) isopropylbenzene
(b) p-xylene
(c) tetralin
Triphenylmethanol is insoluble in water, but when it is treated with concentrated sulfuric acid, a bright yellow solution results. As this yellow solution is diluted with water, its color disappears and a precipitate of triphenylmethanol reappears. Suggest a structure for the bright yellow species, and explain this unusual behavior.
Phenol reacts with three equivalents of bromine in CCl4 (in the dark) to give a product of formula C6H3OBr3. When this product is added to bromine water, a yellow solid of molecular formula C6H2OBr4precipitates out of the solution. The IR spectrum of the yellow precipitate shows a strong absorption (much like that of a quinone) around 1680cm-1. Propose structures for the two products.
Triphenylmethanol is insoluble in water, but when it is treated with concentrated sulfuric acid, a bright yellow solution results. As this yellow solution is diluted with water, its color disappears and a precipitate of triphenylmethanol reappears. Suggest a structure for the bright yellow species, and explain this unusual behavior.
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