What set of reaction conditions would favor an SN1 reaction on 2-bromo-3-methylbutane? strong nucleophile in an aprotic solvent weak nucleophile in a protic solvent weak nucleophile in an aprotic solvent

Weak nucleophile in a protic solvent favors reaction on 2-bromo-3-methylbutane.

Explanation:

So, weak nucleophile in a protic solvent favors reaction on 2-bromo-3-methylbutane.

it can be observed without changing the identity of the object.

it depends on what substance you're talking about as well as many other factors. in quantum mechanics, the observation of particles affects the observers ability to measure certain properties. for example: you can know the velocity of a particle, but you can't know it's position; or you can know it's position, but not it's velocity. it's like trying to find out where a grain of sand is by throwing other grains of sand at it. once you find out where it is, it's been moved. it's also like trying to find an answer to the question of whether or not a tree falling in a forest makes a sound if nobody is there to hear it. paradoxically, the only way to find out is to be there and hear it.

substituting a hydrogen atom with a halogen in a hydrocarbon:

- the single bond remains single. a is wrong.

- the bond with hydrogen is as strong as with a halogen. c is wrong

- a hydrocarbon is saturated if there is no double bond. we do not know that so d is wrong.

- carbon will always have four valence electrons. e is wrong.

by elimination, the correct answer is b. the boiling point of the new compound increases.