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:
0.402 moles
Explanation:
1 mole NaCl/58.44g Nacl ×23.5g NaCl
grams get cancelled out and you are left with moles
Answer:
Explanation:
Exothermic Reactions
Exothermic Reactions
This means that the energy required to break the bonds in the reactants is less than the energy released when new bonds form in the products. Excess energy from the reaction is released as heat and light. Figure: Chemical reaction: A Hermite reaction, which produces molten iron.
I don’t, but what are Gizmos?
When you encounter a storm drain, gravel surface or pothole.