Question

For the first six blanks, please choose options only from the dropdown menus provided below the pictures.

OMS Low Caucomm tom bra tron book (CH3)3COK (CH3)3COH ??? OMS OK OH ل ا ا т Look at the given reaction and select the most appropriate answer from the dropdown menus to fill in the analysis. The substrate moleculeis a primary (unhindered) leaving group. The nucleophile is a [ Select] nucleophile. And the solvent is [Select] This means the reaction likely follows a(n) [Select] mechanism(s), which will result in the stereochemistry at the reacting center being [Select] due to [Select ] in the mechanism.

Dropdown Menus:

1. methyl, primary (unhindered), primary (hindered), secondary, tertiary

2. poor, weakly basic, strongly basic (hindered), strongly basic (unhindered)

3. protic, aprotic

4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction

5. randomized, inverted, predictable but not inverted, unchanged

6. a planar carbocation intermediate, backside attack transition state, anti-periplanar transition state, other

Answer 1

om ((tts) cok (Ct) Color belo Mechanin. (CH) CE & The substrit nde.cull af primary onhinderea & * Nucleophile a strongly banic Chindered) solvent - Drotic solvent Reaction follows y Ez ... predict the sut not inverted, anti periplanar transition state & & & Scanned with CamScanner