When Sn2 reaction takes place at stereogenic site the inversion of configuration takes place with the formation of trigonal bipyramidal type of transition state which is very unstable.
Describe, in a step-wise manner, what happens to a stereogenic center containing a halide during the...
A. Explain why tosylates make good leaving groups. B. What is the orientation of the stereogenic center after the reaction depicted in the figure? н 1. Cl-Ts, pyridine он (R) 2. SCH3, THF The addition of an acid to an oxirane ring is one of the more non traditional mechanisms in the chapter. Using the posted example, explain, in a stepwise manner, what happens in the mechanism. Be sure to comment on why we see a nucleophile add to the...
Write the complete step-wise arrow.pushing mechanism for reaction shown below. Show electron flow with arrows, and be sure to include all intermediate structures. You must be very detailed in your mechanism for full credit. H2SO4
Write the complete step-wise arrow-pushing mechanism for reaction shown below. Show electron flow with arrows, and be sure to include all intermediate structures. You must be very detailed in your mechanism for full credit. HO -CH₂CH₃ CH2CH3 -CH2CH3 CH2CH3 H2SO4
5. [5 pts] Use curved-arrow notation to write out a detailed, step-wise mechanism for the reaction listed below. Be sure to (a) include all of your lone pairs, (b) include all formal charges, (c) draw your arrows neatly and precisely, and (d) enclose intermediates within square brackets. If you get stuck, number the atoms of your reactant and the corresponding atoms in your product to help recognize what bonds are made and broken! HBr r Mechanism: +4 +
Step by step please
- 3 10 2 40 300 10 7. Describe what happens during the coagulation and flocculation process of conventional water treatment
Alkyl halides may undergo elimination reactions with BrØnstead-Lowry bases in which the halide and an adjacent proton are lost to form a new π bond. Because of the loss of a proton and a halide anion the reactions are termed ‘dehydrohalogenation’. The two most common associated mechanisms are designated as either unimolecular (E1) or bimolecular (E2) elimination reactions based on reaction rate studies. E1 reactions proceed via a two-step mechanism that involves the cleavage of the leaving group (here the...
16. [10 pts) Use curved-arrow notation to write out a detailed, step-wise mechanism for the following transformation. Be sure to (a) include all of your lone pairs, (b) include all formal charges, (c) draw your arrows neatly and precisely, and (d) enclose intermediates within square brackets. (If you get stuck, number the atoms of your reactant and the corresponding atoms in your product to help recognize what bonds are made and broken!)
State the condition of instability for and describe what happens during a β+ decay
Alkyl halides may undergo elimination reactions with BrØnstead-Lowry bases in which the halide and an adjacent proton are lost to form a new π bond. Because of the loss of a proton and a halide anion the reactions are termed ‘dehydrohalogenation’. The two most common associated mechanisms are designated as either unimolecular (E1) or bimolecular (E2) elimination reactions based on reaction rate studies. E1 reactions proceed via a two-step mechanism that involves the cleavage of the leaving group (here the...
Physiology: Describe what happens during a heartbeat. Include what muscles contract when and what causes those contractions, what happens to blood within the heart during different parts of the beat, and what you would observe on an ECG during each part of the beat.