Answer:
D would be the best answer
Explanation:
Answer:
-) 2-methylbut-2-ene
-) 2-methylbut-1-ene
-) 3-methylbut-1-ene
Explanation:
in this case, the hydration of alkenes is a <u>marknovnikov reaction</u>, this means that the "OH" group would be added in the <u>most substituted carbon</u> of the double bond. (Figure 1)
For 2-methylbut-2-ene the most substituted carbon is the <u>tertiary carbon</u> (the carbon in the right of the double bond), so we will obtain the desired molecule. In 2-methylbut-1-ene the most substituted carbon is again the <u>tertiary carbon</u> (the carbon in the bottom of the double bond), so we will obtain 2-methyl-2-butanol. Finally, for 3-methylbut-1-ene the carbocation would be formed on carbon 3, this is a secondary carbocation. We can obtain a most stable carbocation if we do a <u>hydride shift</u> (Figure 2). With this new molecule is possible to obtain 3-methylbut-1-ene.
redox- noun- a process in which one substance or molecule is reduced and another oxidized; oxidation and reduction considered together as complimentary processes.
example- "redox reactions involve electron transfer"
Answer:
Energy transfer between the particles in solids, liquids, and gases can explain how warm matter outside a cup can cause a cold liquid inside the cup to warm up.
Explanation: