can someone show me how to do this and explain this to me 18. The species...
can someone show me how to do this and explain this to me 19. The species shown below represents the transition state for the: CH2CH3 H2O ----C----- Br 8+ 8 нн reaction of 1-propanol with HBr. reaction of 1-bromopropane with OH. addition of HOBr to 1-propene. addition of HBr to propene with peroxides.
The species below shows the transition state for the The species shown below represents the transition state for the CH2CH3 HIO ---C---- Br 6 HH A) reaction of 1-propanol with HBr. B) reaction of 1-bromopropane with OH". C) addition of HBr to propene with peroxides. D elimination of HBr from 1-bromopropane.
I don't know what is the correct answer and try to find it in book but I couldn't find it The species shown below represents the transition state for the reaction of 1-propanol with HBr. reaction of 1-bromopropane with OH^-. addition of HOBr to 1-propene. addition of HBr to propene with peroxides.
can someone show me how to do the work and explain it to me 12. Which of the following does not correctly describe Sn2 reactions of alkyl halides? Tertiary halides react faster than secondary halides. Rate of reaction depends on the concentrations of both the alkyl halide and the nucleophile. The mechanism consists of a single step with no intermediates. The transition state species has a pentavalent carbon atom.
can someone show me how to do the work and explain it to me 12. Which of the following does not correctly describe NZ he following does not correctly describe SN2 reactions of alkyl halides? B. Tertiary halides react faster than secondary halides. e or reaction depends on the concentrations of both the alkyl halide and the nucleophie. The mechanism consists of a single step with no intermediates. The transition state species has a penta valent carbon atom.
can someone show me how to do the work and explain it to me 9. A pentacoordinate carbon is a transient species in the mechanism. SNI SN2 EI E2 C. D.
can someone please explain how to do this with as much detail as possible. someone tried to explain it earlier in relation to (a,e) and (e,a) but im not sure even what that means Bccurance of Methyl shift o. The following two elimination reactions are found to have very different rates of reaction. The cis compound produces two products and it reacts much faster than the trans isomer, which produces only one product. Explain these observations (the erence in rate...
can someone show me how to do the work and explain it to me 8. Which of the following reacts fastest with methanol by the SNI mechanism? A) CH2CH2CH2CH2CH2Br B) CH2CH2CH2CHCH3 Br C) (CH3)2CCH2CH3 Br D) (CH3)3CCH2Br
can someone show me how to do this and explain this to me 22. In which of the solvents below would the reaction shown take place at the fastest rate? CH2CH.CH.CH,CN + NaBr A. CH3CH CHCHBr + NaCN ethanol acetic acid dimethyl sulfoxide water
can someone show me how to do the work and explain it to me TIEM210-W03, Fall 2019 Prof. J. Fiorito 13. What is the rate limiting step in the following reaction? (CH3)3CCI + H2O - (CH);COH + HCI A) (CH3)3CCI -- (CH3)3C' + cr B) (CH3)3C + H2O - C) (CH3),C-OH + H20 - D) H0+ + cr H (CH3)3C-OH, (CH3),COH + H30 Cl + H20