The tert-butyl chloride in ethanol would surely react faster than the solvolysis of 1-chloro-2,2-dimethyl propane. It is known that both reactions are under the SN2 category so it would be hard for these reactions to occur. However, SN1 reactions are possible because of the ethanol which is a polar solvent. Both would form carbocations but tert-butyl chloride forms a more stable carbocation while the 1-chloro-2,2-dimethyl propane forms a primary carbocation only.
The monochloroderivatives will be obtained by substituting chemically non equivalent hydrogen with chlorine atom, one by one
So the possible monochloro derivatives of 2,4-dimethylpentane (figure 1) are shown in figure (2)
Hello!
The process in which hydrogen nuclei combine with each other to form helium and other heavier elements is called Nuclear Fusion.
Nuclear Fusion happens when the repulsion between the two nuclei is overcome by the Strong Interaction Force, spending and releasing high amounts of energy.
The two nuclei need to be close enough for Nuclear Fusion to happen, and the energy needed to achieve that is given by the extremely hot temperatures that exist within stars (about 15 000 000 Kelvin). That's why this kind of reactions are common in stars.
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