HCI

Draw the full electron pushing mechanism for the reaction depicted including ALL intermediates (with lone pairs and formal charges). Clearly label the electrophile and nucleophile in each step where appropriate.

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Rank the following intermediates in order of increasing stability.

Rank the following from most reactive to least reactive in an SN1 reaction.

What other alkene is also formed along with Y in Sample Problem 9.3? What alkenes would form from X if no carbocation rearrangement occurred?

Draw tructu f he ajor rganic roduct f he ollowing reaction. CH2 1. Hg(OAc)2, H20 2. NaBH4 CH3 • In cases where there is more than one answer, just draw one. •You do not have to consider stereochemistry. [ド

Classify each carbocation as primary, secondary, or tertiary. a. b. 人 C. d.

Consider the reaction below. Select all of the statements that are true for this type of reaction. OH conc. H2SO4 heat The reaction occurs via the antiperiplanar conformation. The reaction is concerted. A key intermediate controls the stereochemical outcome of the reaction The reaction results in racemization. The reaction proceeds only with inversion. The reaction is stepwise.

Could someone help me rank these in order of increasing reaction in an SN1 reaction? Thank you!