Answer:
endoplasmic reticulum (ER)
Answer: Well!
Explanation: I was going to answer D but fverdell82156 got to it first! So I have to agree with him! It is D!
Answer:
IV
Explanation:
The complete question is shown in the image attached.
Let us call to mind the fact that the SN1 mechanism involves the formation of carbocation in the rate determining step. The order of stability of cabocations is; tertiary > secondary > primary > methyl.
Hence, a tertiary alkyl halide is more likely to undergo nucleophilic substitution reaction by SN1 mechanism since it forms a more stable cabocation in the rate determining step.
Structure IV is a tertiary alkyl halide, hence it is more likely to undergo nucleophilic substitution reaction by SN1 mechanism.
The temperature, pressure and volume of a gas are all related
The result when the OH- ions go as additional acid is added is that t<span>hey remain in solution but change concentration. </span>This is because when you add more acid to hydroxide, it will change its concentration due to the acidity added.