Compare and contrast SN1, SN2, E1 and E2 reactions. What are some obvious similarities and differences between each reaction pathway? What are the requirements for each reaction to work? Discuss why SN2 is in direct competition with E2 while SN1 is in direct competition with the E1 reaction pathway. What is the rate expression for each? Which reactions are concerted? Which reactions are step-wise? Which reactions are stereospecific and what is the stereospecificity of each that are? How do the variables below help influence which reaction pathway will lead to the major product formed?
a. Substrate (substitution pattern and leaving group ability) b. Nucleophile/base strength (weak or strong) and size (unhindered or hindered) c. Solvent (polar-aprotic or polar-protic) d. Temperature (low/ambient temps vs. higher temps)
Compare and contrast SN1, SN2, E1 and E2 reactions. What are some obvious similarities and differences...
1) Compare and contrast SN1, SN2, E1, and E2 reactions! (similarities abd differences. Requirements for each to work.) 2) Why is SN2 is in direct competition with E2 while SN1 is direct competition with E1 reaction. 3) Rate expression of each 4) which reactions are concerted? Which are atep wise? 5) which are sterospecific and what stereospecificity of each are? 6) how do the variables below (A-D) influence reaction pathway? Compare and contrast SNI, SN2, El and E2 reactions. What...
Look at the given reaction and select the most appropriate answer from the dropdown menus to fill in the analysis. The substrate haloalkane is a ["methyl", "primary (unhindered)", "primary (hindered)", "secondary", "tertiary"] haloalkane. The nucleophile is a ["poor", "weakly basic", "strongly basic (unhindered)", "strongly basic (hindered)"] nucleophile. And the solvent is ["protic", "aprotic"]. This means the reaction likely follows a(n) ["SN2", "SN1", "E2", "E1", "SN2 and E2", "SN1 and E1", "No reaction"] mechanism(s), which will result in the stereochemistry at...
Organic chemistry help: Of the four reactions SN1, SN2, E1, and E2; which are capable of occurring with the attached structure? You may use any nucleophile, base, or solvent system of your choosing. Hint: look at the mechanism for each reaction type. Br Of the four reactions SN1, SN2, E1, and E2; which are capable of occurring with the attached structure? You may use any nucleophile, base, or solvent system of your choosing. Hint: look at the mechanism for each...
Dropdown Menus: 1. methyl, primary (unhindered), primary (hindered), secondary, tertiary 2. poor, weakly basic, strongly basic (hindered), strongly basic (unhindered) 3. protic, aprotic 4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction 5. randomized, inverted, predictable but not inverted, unchanged 6. a planar carbocation intermediate, backside attack transition state, anti-periplanar transition state, other CH3CH2ONa ??? CH3CH2OH Br OH OH OH De on an or rega ang Look at the given reaction and select the most appropriate...
HWS 5: Due 10/30/2019 15 points total SN1, SN2, Elimination pt 1 1. (10 pts) For the following reactions: a. Label the Nucleophile (Nu) and whether it is strong or weak b. Label the Electrophile (E) and whether it is primary, secondary, or tertiary and circle the leaving group C. Label the Solvent and whether it is polar protic or polar aprotic d. Categorize each as preferring SN1, Preferring SN2, or could do either e. Draw the product of the...
Look at the given reaction and select the most appropriate answer from the dropdown menus to fill in the analysis. Choose one of the answers in the bracket: The substrate haloalkane is a ["methyl", "primary (unhindered)", "primary (hindered)", "secondary", "tertiary"] haloalkane. The nucleophile is a ["poor", "weakly basic", "strongly basic (unhindered)", "strongly basic (hindered)"] nucleophile. And the solvent is ["protic", "aprotic"] . This means the reaction likely follows a(n) ["SN2", "SN1", "E2", "E1", "SN2 and E2", "SN1 and E1", "No...
8. complete the following reactions. mention the type of mechanism (SN1,SN2, E1, or E2) that each follows 8. Complete the following reactions. Mention the type of mechanism (SNI, SN2, E1 or E2) that each reaction follows. (4) (CHy)COH 100°C Br a) Cl Xiocn, NaOCH3 Heat CH3 b) Cl CH3ONa CH3OH,100°C CH3
If you desire to perform a "clean" E2 reaction, which of the following factors helps avoid competition with SN2 mechanism? a. use of a polar solvent b. use of a hindered bulky base c. use of a good nucleophile d. use of a good leaving group Alcohol dehydration is mechanistically an: a. SN2 reaction b. E2 reaction c. E1 reaction d. SN1 reaction
Identify whether each of the following reactions occurs through an SN1, SN2, E1, or E2 mechanism. Identify whether each of the following reactions occurs through an Sn1 , Sn2, E1, or E2 mechanism.
which substitution and elimination reactions follows Zaitsev’s rule? SN1, E1, SN2, E2?