In contrast to #2, when neopentyl bromide, (CH3)3CCH2Br, spontaneously ionizes, it does NOT result in the expected neopentyl cation (CH3)3CCH2+, but something else. Show this. Warning: this is a two step reaction. Show both mechanisms.

because u need two or more forms of the same element that contain equal numbers of protons but different numbers of neutrons in their nuclei to form isotopes.

so since they all have the same shape? i mean maybe because m& m and reeses are both chocolates

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.

the answer is a for sure mark brainliest i had got this right on usatestprep