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- 29) Draw all of the expected products for the following reaction. Circle the most dominant product in each reaction. 'BUOK 3 NaOEt2. Draw the mechanism for this reaction H2SO4 НоQue Draw the major product of this reaction. Ignore inorganic byproducts. (CH3)3CCI (1 equiv) AICI3 P Type here to search Lenovo Esc 且十 F1 F2 F3 F4 F5 F6
- ↑ ... Propose a reasonable stepwise mechanism, using curved arrow notation to show the flow of electrons, for the following reaction. KCN H EtOH, H₂O OH 02N O₂N NO2 Tt O ọ ♡ > Ր5) Use a curved arrow notation mechanism to show how each product is formed in the following reaction. Iderstity-themejor prodret. 0H HzO Br OH1. Draw the mechanism and products for the following synthetic sequence. OH 1) TMSCI, Et3N Br 2) Mg 3) Acetone 4) H₂O 5) TBAF
- Draw complete mechanism (including intermediates) for each polar reaction below.This content is protected and may nag shared t 4. Consider the following reaction. This reaction is a multi-step reaction. [1] Draw the mechanism for each step of this reaction using curved arrow notation, include all lone pairs of electrons if they are directly involved in the reaction. [2] Identify the arrow pushing pattern (mechanistic pattern: nucleophilic attack, loss of leaving group, or proton transfer) for each step. [3] Draw a transition state for each step. H-OSO3H CH3 00 H H3C-O-H Хосно H3C-O-H Hwhich reagents/mechanism complete this reaction? Solve plzzz!!!
- The following molecules are subject to substitution (SN1 or SN2) reaction conditions. a) Identify if the leaving group (-Br) is attached to a 3°, 2°, 1°, or methyl Carbon. b) Rank the molecule with respect to their SN1 reactivity, with 1 being the fastest and 4 being the slowest. c) Rank the molecule with respect to their SN2 reactivity, with 1 being the fastest and 4 being the slowest. Br Br CH3B Br a. type of Carbon on C-Br b. SN1 reactivity (1 fastest, 4 slowest) c. SN2 reactivity (1 fastest, 4 slowest)Draw the mechanism for this reaction. HO H,SO4.A student attempted to synthesize an epoxide according to the reaction scheme shown here, but no epoxide was formed. Explain why. Hint: It may be helpful to build a OH NaOH No epoxide model of the reactant molecule. (H3C);C' Br