1. It is an example for E2 Elimination and occurs in a single step. Both the departing groups Elimination occurs simultaneously.
And moreover, the base tertiary butoxide is a bulky base and removes proton from less hindered side as below.
2. H+ is a Electrophilic species and electron deficient, attacked by alkene. Hence electrons flow from Alkene carbon to H+ ion.
3. Bromination of alkene occurs via the formation of cyclic bromonium ion by Electrophilic Addition mechanism.
Mechanism: a) Each of the following mechanistic steps, there is one error briefly explain the error...
Q. Predict mechanism type (SN1, E1, SN2, E2) for the following reactions. If more than one is possible, predict which mechanism is more likely and explain why. 5 - HI ح . 0H SNI KOCH2CH3 KOCHCH - I want to wors. NaOH, H2O, 100°C في NaCN ي . HO )..NC دا SN2
3. For the below reaction mechanism, write the correct rate law. K. Học-NHH – HẠNK • HI م | ه HgCeX ح H₃C-NH₂ 4. Rank the following substrates in order of increasing reactivity in an Sn2 reaction. ال اس ام اس
Please include steps within mechanism, first step, second step, etc... Please explain how and why this reaction occurs in the BLACK box? :Br Now, please draw mechanistic arrows in the BLUE box to represent how this reaction occurs. Br: :Br XReset Draw Adjust Erase
Q25 Contrast the bureaucratic/mechanistic organization to the organic organization. a) List and briefly explain the specific activities that are part of directing. [2 Marks] b) List and briefly explain the essential steps in the control process. [2 Marks] c) List and briefly describe the kinds of controls used by managers. [2 Mark d) Describe ways in which a supervisor can coordinate his operations. [2 Marks] DO NOT WRITE THE ANSWERS - USE WORD FORMAT. NO PLAGIARISM IN THE ANSWERS.
Write equations for the mechanistic steps in the dehydration of cyclohexanol assuming an E1 mechanism. What is the role of phosphoric acid? Why is heat required?
Mechanism Practice Complete the elementary steps below by adding mechanistic arrows to show how the product is formed. For some of the reactions, you will need to determine the products as well. Make sure you show all formal charges and all lone pairs that are involved in the mechanism! Nucleophilic Addition H. +HOCH Proton Transfer (intramolecular) Deprotonation (intermolecular OH +
Which of the following mechanistic steps of allylic bromination does the following represent? Br H Initiation Termination via disproportionation Termination via recombination Propagation Hydro-carbo dissociation Carbo-bromo reordination What is the product of the following Diels-Alder reaction? Diels-Alder ? 1 - 0 0 A B D E Ос ОЕ OD A
1. Name the following compounds: ОН o plan 2. Draw the steps of the mechanism for the following reactions and explain each step. no Na + Br Å. LOH HSO4 OH
4. For each of the following elimination reactions (a-c): (15 points) (a) State which elimination mechanism would predominate; briefly explain your choice. (b) Show the mechanism leading to the major elimination product. (a) ОН SNa (b) Br Br NH2 . (c)
2. REAGENTS: Provide the reagents needed to accomplish the following transformations. Clearly indicate if you need to use more than one step. (12 pts.) - گره م . = . . - م م ه م . .. 3. MECHANISMS: Provide complete, arrow-pushing mechanisms for each of the reactions shown below. Only TWO of these will be graded but YOU MUST COMPLETE ALL FOUR TO EARN ANY CREDIT! (8 pts.) | مو | (note: only mechanism for step 1) 1....