Increasing the temperature a reaction takes place at increases the rate of reaction. At higher temperatures, particles can collide more often and with more energy, which makes the reaction take place more quickly. ... Both reactions release a gas and both finish at the same volume .
lol answer this question 3 times
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.
Answer:3 moles of Oxygen atoms weigh 48.00 grams.
Explanation: