Organic chemistry question please help

Amines are converted into akenes by a fwo-step process called the H0/fmann elimination. SN2 reaction of the amine with an excess of CH3 in the first step yields an intermedlate that undergoes E2 reaction when treated with siver oxide as a base. Pentylamine, for example, yields 1-pentene. CH3CH2CH2CH2CH2NH21.excessCH3I2.Ag2OH2OCH3CH2CH2CH=CH2 Propose structures for the intermediate and the alkene produced in steps 1&2 when the following compound undergoes Hofmann elimination C((CH3)3NH2IntermediateAlkene - You do not have to consider stereochemistry. - You do not have to explicitly draw H atoms. - Include anionic counter-ions, e gi is, in your answer, but draw them in their own sketcher. - Separate intermediates from products using the - symbol from the drop-down menu