Part 1 involved MeOH addition to form the key tetrahedral intermediate. Part 2 involves loss of H2O from the tetrahedral intermediate to form the ester. Part 2 of 2: Intermediate species (from Part 1):

For all remaining steps in the mechanism: 1) Draw each species (organic and inorganic) resulting from the previous step. Each step will include all of, and only, the atoms given in the first step (i. e., do not use extra reagent molecules/ions, and do not omit spectator ions).

(Depending on how you drew the mechanism, the drawing area below might not be needed. Do not draw the final products.)

answer: you could do some invislibe ink.

explanation: i will tell you how to if u answer my question.

sorry i was late, but i don't know what assignment your talking about, i'm in flvs as well, im in earth space science. but u are behind pace bc every class should be in the 3's or 4'

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.