1. Which of these will undergo a rearrangement during the reaction2. For reaction D- is HBr the nucleophile or electrophile?3. For each of the reactions :Complete the reaction, showing the mechanism by usingb. Draw the intermediate – showing the carbocation and anDraw and write the name of the final product.To name a compound with a halide attach – treat the halide as a substitueshowing it's placement.Bromine = bromo, Chlorine = chlare, etc.…..HCIb)d)HBr

Answered: 1. Which of these will undergo a…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter20: Acidity And Pka Of Phenols

Section: Chapter Questions

Problem 11E

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For each of the following reactions diagram the steps from the substrate to the product. For each step, a) over the reaction arrow supply the needed reagents b) name the type of reaction/mechanism {ROS (SN1, SN2, radical) E(E1, E2) A [acid-base, addition (carbocation, onium bridge, radical)]}
I labeled one of the atoms incorrectly, but I am not sure which. Would the H in HBr be considered a nucleophile as well ?
Show the SN2 mechanism in the reaction between (S) 2-bromobutane and iodide ion. Label the product and draw a enery diagram for this reaction.
The question is: "Draw the curved arrow mechanism for the reaction between (2S,3S)-3-methylhexan-2-ol and PCl3. Note the specific instructions for each box. Include nonzero formal charges and lone pairs of electrons on all appropriate atoms" I attached screenshots of the picture of the atoms below. What type of reaction (SN1, E1, SN2, or E2) would the reaction be, and how would these molecules interact? The question asks for multiple steps so I am guessing it is either SN1 or E1, but what is the reaction mechanism?
What is the strongest nucleophile, NH3, CH4, CH3O-, or H2O?
I. Of the following reactions, answer what is requested:a) Analyze the type of alkyl halide and determine if the nucleophile is strong or weak and also if it has a basic character.b) According to the previous paragraph, determine if there is competition between the substitution and elimination reactions.c) Describe the mechanism of each of the product (s) that are formedd) Of the product (s) that are formed, indicate which one comes from the substitution reaction and which one from eliminatione) If two or more products are formed, indicate which would be the majority and explain why.
For SN1 Explain if 3o ( tertiary) alkyl halides reacted (fastest or slowest) explain why. Be sure to explain if alkyl halides did not react or did react and why. 3o (tertiary) compounds listed are: 2-chloro-2-methylpropane (see picture) Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature.
Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol or enone below. You do not have to consider stereochemistry. Draw the enolate ion in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu.
- The reaction that will be carried out in the lab will convert 9-fluorenol to 9-methoxy fluorene usinga nucleophilic substitution reaction. Question: Why is concentrated sulfuric acid used in this reaction and not aqueous acid? Draw the reaction and show the equilibrium that is dependent on the acid.
What are the list of difference between SN1, SN2, E1, and E2? (such as the type of nucleophiles needed, the type of substrates, solvents etc.)
What are the list of difference between SN1, SN2, E1, and E2? (such as the type of nucleophiles needed, the type of substrates, solvents etc.) When do we know when to use which mechanism? How do we use heat in an elimination reaction?
From each pair, select the stronger nucleophile. Q.) CH3SH or CH3S-

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