The correct answer is
b.tert butyl bromide
because after leaving group Bromo there will be formation of stable carbocation. And react faster
E1 indicates a elimination,unimolecular reaction, where rate = k [R-LG]. In an E1 reaction, the rate determining step is the loss of the leaving group to form the intermediate carbocation. The more stable the carbocation is, the easier it is to form, and the faster the E1 reaction will be.
Jestion 14 tot yet answered Which of the following structures will react fastest in uni-molecular elimination...
1. Given the following structures that react by Sn1, which would react fastest and which would react slowest. Give reasoning. 5-bromo-1,3-pentadiene, bromocyclopentane, (R)-2-bromo-2-methylhexane. 2.If bromocyclohexane reacts faster than chlorocyclohexane in an Sn2 reaction, what could be the reason? 3.You wish to substitute the bromine in the following molecules with a nucleophile. Explain whether the given molecule would react by Sn1 or Sn2 mechanism and explain why. 1-methyl-1-bromo-cyclohexane, 1-bromopropane, 2-bromohexane. 4. Why does benzyl bromide react under both Sn1 and Sn2...
Which of the following molecules has a zero dipole moment? on 36 Not yet answered Select one: Marked out of 5.00 O a none of these P Flag question O b. XeF2 c. NCI d. H2S De ICI Select the correct molecular structure for NH! uestion 37 ot yet swered Select one: a. arked out of 10 linear Flag question b. of these 37 Select the correct molecular structure for NH3. Select one: out of a. linear Jestion b. none...