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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 NaOEtQue 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 F62. Draw the mechanism for this reaction H2SO4 Но
- ↑ ... 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 OHDraw complete mechanism (including intermediates) for each polar reaction below.
- 1. Draw the mechanism and products for the following synthetic sequence. OH 1) TMSCI, Et3N Br 2) Mg 3) Acetone 4) H₂O 5) TBAFThis 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 HThe 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)
- which reagents/mechanism complete this reaction? Solve plzzz!!!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