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- Show me the mechanism of this reaction using only 1 bromination. *R listed is NHCOCH3.Match the questions with the correct descriptions below: Sn2, E2 E1cb Sn1, E1 (anti) E2, E1cb Sn1, E1 2 steps poor leaving group 2 carbons removed from a carbonyl group carbanion intermediate 3°>allylic, benzylic>2°>1°>CH₃ carbocation intermediate Ist order reaction (r=k[RX]) H-X anti no intermediate 2nd order reaction (r=k[RX][Nu]) polar aprotic solventNeed help with part c. The cyclohexane derivative shown below does not undergo E2 elimination. what do we do after we roate the bond roate the bond.
- 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:Draw Sn1/E1 products of both reactions below or fill in the blank with appropriate stuffs for Sn1/E1Which of A to E shows the structure of the major product obtained from the E1 reaction shown below?
- E1 Reaction- Solvolysis gives 5 products. Consider both carbocations and draw all 5 products.Tertiary alkyl halides will react by E2 under neutral conditions under acidic conditions under basic conditions will not react by E2Rank the following in increasing order of reactivity towards nucleophilic acyl substitutiona. CH3COCl, CH3COOCH3, CH3CONH2b. CH3COOCH3, CH3COOCH2CCl3, CH3COOCH(CF)3
- 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?Draw all possible alkenes that could be generated from an E2 elimination reaction of 3-bromo-3-methylhexane. Suggest conditions that can be used to make just one of the alkenes in a controlled manner (i.e., conditions that would lead to formation of just one alkene as the major product).Minor product via E1 for 2-butanol and HCl?