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- Please show the entire mechanism with curved arrows for the reaction. Why is the reaction considered unfavorable in reference to the stability ladder? Why does the reaction favor the product formation? *please show the resonance structures in the reaction.*what is the rate at which Br- (aq) disppears in reaction below if the rate of disappearence of BrO3- (aq) is 0.022 M/swhat is a possible mechanism for the following reaction ??
- Step 4c: Draw the resulting structure or structures indicated by the curved‑arrow mechanism shown. Include formal charges, but not lone pairs.Following is a balanced equation for bromination of toluene.(a) Using the values for bond dissociation enthalpies given in Appendix 3,calculate ∆H0for this reaction.(b) Propose a pair of chain propagation steps and show that they add up to theobserved reaction.(c) Calculate ∆H0for each chain propagation step.(d) Which propagation step is rate-determininRank the reactivity of these below: most reactive (1) and least reactive (3)
- Arrange the following according to INCREASING reactivity towards E2: 1st ( least reactive)? 2nd? 3rd? 4th (most reactive)?Pls ignore the highlighted part __________ is reduced in thefollowing reaction: Cr2O72- + 6S2O32-+ 14H+→ 2Cr3+ + 3S4O62- + 7H2OCan you do 3 and 4 and explain it? And how yo identify it. State the mechanism in which through reaction proceeds sn2 or sn1
- What carbon radical is formed by homolysis of the C–Ha bond inpropylbenzene? Draw all reasonable resonance structures for thisradical.i) Ph2PH ii) Nal iii) PhCH2OH iv) CH3SH v) Pr2CuLi At what letter in the picture will each above subtrate react on? (A/B/C)Which reaction is faster, one with Eact = +41.8 kJ/mol or one with Eact = +20.9 kJ>mol? Explain.