G 5% Carbocation Rearrangements 7) Draw the 5 MOST LIKELY carbocation rearrangements of the following intermediate. Bonus: Put an X next to the least likely structure and briefly explain why. alk of
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- Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. Do not include the halide anion. Let Marvin JS adjust the number of hydrogens automatically as you use the charge tool to specify formal charge. + HCI Marvin JS - Troubleshooting Marvin JS - CompatibilityDraw the equilibrium chair confirmation of cis1-chloro-3-methylcyclohexane. Interpret the E2 elimination, and draw the structure of the product!The cis isomer of 1-bromo-4-tert-butylcyclohexane undergoes E2 elimination about 1,000 times faster than the trans isomer. Explain why the cis isomer reacts faster. Hint: It is not because of steric hindrance. Br + NaOH Fast (H3C),C (H3C);C Br + NaOH Slow (H3C);C' (H3C);C
- What are the possible constitutional isomers and rank by SN2 reaction.1. SN1 or SN2 2. Include major product and stereochemistry 3. Add detailed reaction mechanismsIn the E2 reaction of 2-bromopentane with sodium tert-butoxide, 1-pentene is favored over 2- pentene. It is based on O the size of base used. O the Zaisev's rule. O the strength of the base used. O the Hoffman product. O the stability of alkene
- 1. please answer a and b3. Draw the complete mechanism and use the mechanism to predict the major product(s). Include stereochemistry where appropriate. a. b. H-Br -78 °C H-Br -78 °C H-Br 40 °Cb) Circle the major product for the following reaction. CH,CH,CI -C- H2 O2N AICI; O2N- O2N- H2 H2 II O2N- O2N H2 H2 III IV