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- Q7 Consider the reaction, where the alkane shown is subjected to radical bromination at 25 °C. Br₂ light Describe the major monobromination product. productFor each reaction, decide whether substitution or elimination (or both) is possible, andpredict the products you expect. Label the major products. chlorocyclohexane + NaOC(CH3)3 in (CH3)3COHThe major product formed by addition of HBr to (CH3)2C=CH– CH=C(CH3)2 is the same at low and high temperature. Draw the structure of the major product, and explain why the kinetic and thermodynamic products are the same in this reaction.
- Determine which carbocation rearrangements you drew for Problem 7.36 produce a significantly more stable carbocationthan the reactant.||| IV Identify the least stable carbocation. A) I B) II C) III D) IVA carbocation intermediate is central to which of these reaction types? E1, E2, SN1, SN2 ? Choose 1
- (R)-2-chloropentane was reacted with NaSCH3. The compound yielded 65% (S)-2-chloropentane with the enantiomer making up the other 35%. Which mechanism was followed in the reaction? Both, more SN2 Both, more SN1 SN1 SN2What is the product (A, B, C, or D) of the reaction shown in Image30? a. C b.D c. B d. AKk.174. Please fill out this reaction mechanism with the missing reagents and intermediate products with a complete arrow-pushing mechanism.