Consider the SN2 reaction between 1-bromo-2-methylpropane and methoxide. Add curved arrows to the starting materials to indicate the flow of electrons. Draw the product species to show the balanced equation, including nonbonding electrons and formal charges. H₂ H3C H C - Br: + :0-CH3 product CH3 Draw curved arrows. Select Draw Templates More // C Br 0 H₂C EC CH₁ - Br Draw the products. The bromide ion has been drawn for you. Erase : 0— CH, Select Draw Templates More ///// C Br 0 Erase
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- -Name the correct mechanism via arrow pushing -name each mechanism -name each minor and major products (1R,2S)-1-iodo-2-methylcyclohexane + ethanol/DMSO/stirred 3 daysshow all important steps of rxn. (3S,4R)-2-bromo-3-propyl-2- phenylpentane in ch3OH. label arrow, intermediates, and all potential priducts1. Which of the following is the strongest nucleophile? Refer to the diagram below with an MeOH, MeSH, etc. 2. Which of the following is true about the stereochemistry of SN1 reaction?a.retention of configuration at the electrophilic centerb.50:50 mixture of retention and inversion of configuration at the electrophilic centerc.inversion of configuration at the electrophilic centerd. slightly more inversion than retention at the electrophilic center
- Consider the series of the trans effect: CO, CN-, C2H4 > PR3, H-, CH3- > C6H5- > NO2-, SCN-, I- > Br- >Cl- > py > NH3 > H20 What would be the major product of the following reaction? Select one:Please complete boxed reactions. Thanks. P.s. this is not graded work but a study guide.Draw the molecule: Under second-order conditions (strong base/nucleophile), SN2 and E2 reactions may occur simultaneously and compete with each other.Show what products might be expected from the reaction of 2-bromo-3-methylbutane (a moderately hindered 2∘∘ alkyl halide) with sodium ethoxide. Do not worry about sterechemistry inther SN2 product for this problem. Don't forget about stereochemistry.
- Adjust the structures below to show the resulting intermediates.Rearrangements can occur during the dehydration of 1° alcohols eventhough no 1° carbocation is formed—that is, a 1,2-shift occurs as the C—OH2+ bond is broken, forming a more stable 2° or 3° carbocation, asshown in Equation [1]. Using this information, draw a stepwisemechanism for the reaction shown in Equation [2]. We will see anotherexample of this type of rearrangementAssume that 2-chloropropane reacts with CN− in an SN2 reaction. Use the JSME editor () to draw the structure of the substitution product of the reaction. The guide on how to draw your structure can be found here Important Note: When drawing the structures in the JME editor please adhere to the following formats: 1. If the nucleophile is OH−, DO NOT manually add the "H" to the final product 2. If the nucleophile is CN−, be sure to include the appropriate bonding between the C and N in the final product
- Show arrows, mechanism and product of TiCl4 + CH3-O-CH3.Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?Can someone please help me with 2 mechanisms? One is for the synthesis of 1-bromobutane, and the other is for 2-bromobutane. The attached reaction shows the reagents and starting product.