Answer:
Seafloor spreading is a process that occurs at mid-ocean ridges, where new oceanic crust is formed through volcanic activity and then gradually moves away from the ridge.
Explanation:
Mid-ocean ridges and seafloor spreading can also influence sea levels. As oceanic crust moves away from the shallow mid-ocean ridges, it cools and sinks as it becomes more dense. ... Seafloor spreading proves that the ocean itself is a site of tectonic activity.
Answer:
See the explanation
Explanation:
In this case, we have to remember that in the <u>monochlorination products</u> we only have to add one "Cl" with this in mind, we can have several options.
<u>a) 1-chloro-2,2-dimethylbutane</u>
<u>b) (R)-3-chloro-2,2-dimethylbutane</u>
<u>c) (S)-3-chloro-2,2-dimethylbutane</u>
<u>d) 1-chloro-3,3-dimethylbutane</u>
Additionally, from these 4 molecules, we will have 2 enantiomers. (R)-3-chloro-2,2-dimethylbutane and (S)-3-chloro-2,2-dimethylbutane.
See figure 1
I hope it helps!
The question is incomplete, the complete question is;
Indicate which reaction will occur faster. Explain your reasoning. Select the single best answer Hexyl chloride or cyclohexyl chloride with sodium azide in aqueous ethanol O Cyclohexyl chloride reacts faster because it is more soluble in the solvent OHexyl chloride reacts faster because it is less sterically hindered. O Cyclohexyl chloride reacts faster because its carbocation intermediate is more stable. Hexyl chloride reacts faster because hydrogen abstraction is more likely to occur in this compound.
Answer:
Hexyl chloride reacts faster because it is less sterically hindered.
Explanation:
Now we have to think through the problem carefully. We must remember that the azide ion is a good nucleophile. Being a good nucleophile, we should be thinking about an SN2 reaction mechanism.
Though ethanol is a polar protic solvent which may weaken the nucleophile by hydrogen bonding, the nucleophile will still react very fast with a primary alkyl halide such as hexyl chloride via SN2 mechanism.
The substrate is easily accessible to the azide ion in hexyl chloride compared to cyclohexyl chloride hence hexyl chloride reacts faster than cyclohexyl chloride.
U should use B to find out
