The correct answer is option (d). As LiAlH4 is strong reducing agent it will make tertiary alcohol more easily which is most stable alkane.
Which of the following triflates will undergo a faster reaction with LiAlH4? °ore
Which substrate will undergo the transformation faster according
to the following mechanisms?
Which substrate will undergo the transformation faster according
to the following mechanisms?
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which of the following reactions would undergo SN2 reaction faster ? explain your choice a) CH3I + HONa ----> b) CH3I + HSNa ----> thank you
Predict which of these two compounds will undergo the El reaction faster and why Cl CH,CI 2 10. Explain why the nucleophile's strength is unimportant for an Syl reaction.
Which of the following reactions will undergo an E1 reaction faster? Question 2 Not yet answered Points out of 1.0 P Flag question (a) C (b) (c) (d) Select one: O a. (a) 1-bromopentane O b. (b) E-1-bromo-1-pentene c. (C) 3-methyl-3-bromopentane O d. (d) 3-methyl-3-bromo-1-pentene O e. The two fastest of these will have exactly the same rate constant. True or false: When both an SN2 and an E2 reaction are possible, increasing the temperature of the reaction will speed...
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16. (3) Circle the molecule that will undergo the following reaction faster. Explain your reasoning. Br Br H2O or
IV. Which substrate will undergo the transformation faster according to the following! mechanisms? SM: SN2: Y vs w
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1. In each of the following, indicate which S2 reaction will occur faster. Explain your reasoning. a. 1-bromo-2,2-dimethylpropane or 1-bromo-3-methylbutane with Nal in DMSO. b. 1-iodopentane with NaN, in ethanol or NaSCH, in ethanol, c. Reaction of isobutyl iodide with NaBr in acetone or in ethanol. 2. In each of the following, indicate which S, 1 reaction will occur faster. Explain your reasoning. a. Reaction of I-chloro-1-methylcyclohexane or 1-chloro-2-methylcyclohexane in aqueous ethanol. b. Reaction of 2-chloropentane or 3-bromohexane...
7. a) Give the expected product in each case. b) circle the reaction that should undergo an S 2 reaction FASTER in methanol. c) Justify the relative reactivity in terms of anion and transition state stabilities. - o - in - - - y x Cl + H2C-S THH - H2C-OH - - - - - x +H3C-O in H3C-OH H H.
Which of the following alkyl halide will not undergo Sul or Sn2 reaction?
U UUUUUMUS UC 10) Which of the following reagents complete the reaction below: A) TSCI, LiAlH4 B) Raney Ni/H2, heat C) NaBH4, CH2CH OH D) Zn/Hg, HCI