Give the reagent and the reaction conditions that would distinguish between the following compounds. Explain the principles behind the reactions. Write the chemical equation for the reactions involved. 2-methylbutan-2-ol and 2-methylpropan-ol
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- When trans-2-chloro-1-cyclohexanol is treated with a base, cyclohexene oxide is the product. However, when cis-2-chloro-1-cyclohexanol is treated with a base, the product is cyclohexanone A.Write the equation for the reaction between trans-2-chloro-1-cyclohexanol and the base to yield the cyclohexene oxide B.Why doesn’t the cis isomer yield the oxide? C.Write the mechanism for each of the two reactions.When trans-2-chloro-1-cyclohexanol is treated with a base, cyclohexene oxide is the product. However, when cis-2-chloro-1-cyclohexanol is treated with a base, the product is cyclohexanone i. Write the equation for the reaction between trans-2-chloro-1-cyclohexanol and the base to yield the cyclohexene oxide. ii. Why doesn’t the cis isomer yield the oxide?. iii. Write the mechanism for each of the two reactions.When trans-2-chloro-1-cyclohexanol is treated with a base, cyclohexene oxide is the product. However, when cis-2-chloro-1-cyclohexanol is treated with a base, the product is cyclohexanoneWrite the equation for the reaction between trans-2-chloro-1-cyclohexanol and the base to yield the cyclohexene oxide Why doesn’t the cis isomer yield the oxide?Write the mechanism for each of the two reactions. .
- When trans-2-chloro-1-cyclohexanol is treated with a base, cyclohexene oxide is the product. However, when cis-2-chloro-1-cyclohexanol is treated with a base, the product is cyclohexanone. 1. Write the equation for the reaction between trans-2-chloro-1-cyclohexanol and the base to yield the cyclohexene oxide. 2. Why doesn't the cis isomer yield the oxide? 3. Write the mechanism for each of the two reactionsFrom the given two compounds in the image, which reagents would differentiate the pair? a. Br2 in CH2Cl2 b. CrO3, H2SO4, acetone c. concentrated HCl with ZnCl2 d. aqueous FeCl3 e. aqueous NAHCO3 f. ammoniacal AgNo3Write the structures of the products when Butan-2-ol reacts with the following:(a) CrO3(b) SOCl2
- Give the name of the major organic product formed by the following reaction:1.Give the common name of 2,2-dimethyl-1-propanethiol and give the complete equation as the compound is exposed to oxidation. 2.What will be the product of the compound in #1 if added with NaOH?Consider the structure of cyclohexene, if it undergoes epoxidation followed by exposure to water, which of the following final product is formed? a. Cyclohexan-1,2,-diol b. Cyclohexane c. Cyclohexanone d. Hexan-1,-6-dioic acid
- describe how the following conversions could be carried out. In each case give reagents and conditions of the reactions and the structures of the products. a) CH2=CH2 -> CH2 COOH b) ethanol -> 2hydroxypropanoic acidPredict which member of each pair will be more soluble in water. Explain the reasonsfor your answers. 3-ethylhexan-3-ol or octan-2-olIndicate the necessary reagent and reaction conditions to distinguish the following compounds. Using the appropriate chemical equation, explain how each reagent or condition would react with each compound. 1-butyne and 2-butyne toluene and 1-methylcyclohexene