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- 5. Each of the following may participate in an elimination reaction, under the proper conditions. (a) Circle the alpha (a) carbon. (b) Circle the beta (B) carbon(s). (c) Draw the alkene product(s) that may form, with the new double bond between the a and B positions. (d) If more than one alkene product is possible, circle the most stable (Zaitsev) product. X tx + 3g) Draw the arrow pushing mechanism and predict the product of the reaction. What do we call this mechanism? H3C Br CH3 NaOHGive IUPAC names for the following structures. When appropriate, abbreviate ortho (o), meta (m), and para (p), no italics, if you elect to use these terms. CH₂CH₂CHCHCHSCHCH₂ I T CH₁ CH₂ 1st structure: CH3 CH3 I 2nd structure: Submit Submit Answer Try Another Version OCH3 CH₂CCH₂ OCH3 10 item attempts remaining
- Draw the least stable resonance form for the intermediate in the following electrophilic substitution reaction. CF3 CF3 Br2/FeBr3 • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. Br In cases where there is more than one answer, just draw one. Br F ?Draw the electron-pushing mechanism for the propagation steps of the allylic bromination reactions below. You may omit NBS in your mechanism, and use Br and Br2.Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. H N. Br2 Br • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. IZ
- Considering stereochemistry, draw the resulting E2 elimination product when H. is removed. H a Ho III.... H H₂ I jº ·*||||| H X Ś my èWhat are the products of the following reactions if they proceed via the SN1 mechanism?7. Which substituent would be classified as a deactivating ortho/para director in an electrophilic aromatic substitution reaction? a) || -C-OH b) O || -O-C-CH3 c) -CI d) + -NH3