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)

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)

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter8: Addition Via Carbocation

Section: Chapter Questions

Problem 8E

See similar textbooks

Similar questions

The reactants, intermediates, final products, and all curved arrows showing bonds forming andbreaking are collectively referred to as the mechanism of a reaction. For the following reactants: a. Explain why the original statement of Markovnikov’s rule does not help in this case, but themodern restatement of Markovnikov’s rule tells you which carbon will get the X (Cl). b. Show the mechanism of the most likely addition reaction between the reactants.
Rank the following compounds (an SN2 reaction with NaCN) with 1(the fastest reaction) and 4(slowest.)
The SN2 reaction shows a reversible mechanism when the basic strength nucleophile and leaving group are similar, but not when the strength of the nucleophile as a base is greater than that of the leaving group. Explain.
In the box to the left of each reaction below, write the mechanism by which it occurs (could be SN1, SN2, or E1, or even 2 of them). Then draw the product(s).
Determine whether the sollowing are SN1,SN2, E1, or E2 and draw the major product and if more than one can occur, then draw both products
Draw the product of nucleophile substitution , and determine the likely mechanism ( SN1 or SN2
Draw the major 1,2-addition product and the major 1,4-addition product of the following reaction. Which product is formed at a high temperature? Which product is the thermodynamic product?
Heating an alcohol in the presence of sulfuric or phosphoric acid will cause a dehydration to occur: the removal of the elements of water from a molecule, forming an alkene. The reaction usually follows an E1 mechanism. The SN1 pathway is suppressed, both by heating the reaction mixture (more energy promotes the elimination pathway) and by using a strong acid whose conjugate base is a poor nucleophile. Draw curved arrow(s) to show how the alcohol reacts with phosphoric acid.
is this an E1 or E2 mechanism for this reaction? What is the major product and mechanism for it?
Rank the following from most reactive to least reactive in an SN1 reaction.
"Drawing the Product of Inversion in an SN2 Reaction Label the nucleophile and leaving group, and draw the product (including stereochemistry) of the following SN2 reaction.
Can you do 1 and 2 and explain it? State the mechanism in which through reaction proceeds sn2 or sn1