the alkyl halide is tertiary and it undergoes the SN1
and the E2 reaction with NaOCH3,which is strong base and the
products are as follows
possible Substitution and elimination can be competing reactions. Show all the elimination/substitution products of this reaction...
"Complete the reactions showing all Major Products, both substitution and elimination, that can form based on the reaction conditions. Be sure to show stereochemistry where appropriate. Fill in each table with reaction conditions." w upiete the following reactions showing all products, both substitution and elimination, that can form, then circle the MAJOR Foduct(s). Under each reaction, draw the step by step mechanism showing how each porduct is formed. Show or indicate stereochemistry where appropriate. Fill in each table with reaction...
PROBLEM 7-24 1. Predict the elimination products of the following reactions. When two alkenes are possible, predict which one will be the major product. Explain your answers showing the degree of substitution of each double bond in the products. 2. Which of these reactions are likely to produce both elimination and substitution products? (a) 2-bromopentane + NaOCH3 (b) 3-bromo-3-methylpentane NaO (c) 2-bromo-3-ethylpentane NaOH Me (Me= methyl, CH3)
pls answer all Keeping in mind that carbocations have a trigonal planar structure, wwrite a structure for the carbocation intermediate AND write structures for the alcohol (or alcohols) you would expect from this reaction: 1. CH, но H Br Sy1 Which would you expect to be the stronger nucleophile: 2. a) The amid ion (NHi) or ammonia? b) RS or RSH? The reaction of methyl chloride with aqueous sodium hydroxide to produce methanol and chloride ion is essentially irreversible, proceeding...
Characterize the following reactions as Substitution reactions, Elimination reactions, Addition reactions, or Rearrangement reactions? Reaction type? Select one: a. Addition reaction b. Substitution reaction c. Elimination reaction d. Rearrangement reaction
1. (16 points) In each of the following pairs of reactions elimination competes with substitution. Write the starting material and all possible products of the reactions, don't write mechanistic part. Write "elimination is favored for reaction in which elimination products can be obtained in higher yield comparing to the yield of the elimination product/s in the second reaction. Provide the reason for such statement, reason is in reaction conditions. You can write an opposite statement to the previous one, you...
Additional Questions: 16. For the following reactions, identify all the B-hydrogens, draw all possible elimination products, and circle the major elimination product formed. V acetone Br + CH 00 n NaOCH — + NaOCH3 NACH + NaOH POPS 116 lass Activity 10A Elimination (d) M 9 9 Strouw begong blus min Enamornineralobas - Br + NaOEt r uong bola Dolcooters to commotilois s am 900 W610
Draw both the major organic substitution and elimination products. If no reaction is possible, write "no reaction". Please explain how you got your answer. Thanks!
Hll Name: 1. Give the expected products of E2 elimination for each of following reactions with reaction mechanisms (show all attacks with arrows) :: NAOCH Br CH3OH Н NAOCH3 н CH2OH Br
Give the elimination and substitution products of the reactions below, giving the stereochemistry where appropriate. Write your answers on this page. Br AgNO3/H20 н.с A CH2CH3 rearonagmen! Z sn1 7E1 products CI NaOCH3 Ph CH д, сн,он CH-CHз Нас Sub 3 elim 4 рrod
Additional Questions: 16. For the following reactions, identify all the B-hydrogens, draw all possible elimination products, and circle the major elimination product formed. (a) acetone CHоо + Br (b) -CI +NaOCH3 (c) CI NaOH Elimir (dpm6 mot r atnemepnsise1 p n6 26 0s 2 121t d 0ms2 erit 26d meinsrbom 13 na -BreNaOEt buborn tootSTI691 prilloert lo noitsof e