Please help :) Student Name: Class Day/Time: 3. (3 pts) First, draw the major product. Be...
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3. (3 pts) First, draw the major product. Be sure to show correct stereochemistry. Second, draw a mechanism. Use curved arrow notation. Show all electron lone-pairs and formal charges. Hint: ethanol is a protic-nucleophilic solvent. Brą, ethanol
3. (3 pts) First, draw the major product. Be sure to show correct stereochemistry. Second, draw a mechanism. Use curved arrow notation. Show all electron lone-pairs and formal charges. Hint: ethanol is a protic-nucleophilic solvent. Br2, ethanol
Predict the major substitution product(s) and provide a curved arrow mechanism for the formation of the product. H20 Draw the major product(s). Include stereochemistry in your answer. ? Edit Draw step 1. Loss of leaving group. Include lone pairs, formal charges and stereochemistry in your answer. ? Edit Draw step 2. Carbocation rearrangement. Include lone pairs, formal charges and stereochemistry in your answer. dy ? Edit Drawstep 3. Nucleophilic attack. Draw both enantiomers in products if any. Include one pairs,...
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Class DEVI Ime 1. (2 pts) Rank in order of increasing heat of hydrogenation (1 = lowest, least heat reeds west, least heat released; 5 - highest, most heat released). HEC CHE н,с сну 2. (3 pts) Draw a mechanism for the hydration of the alkene below. Be sure to use curved-arrow notation and include all electron lone pairs and all formal charges.
Draw a major resonance structure for the following enolate. Use
curved arrows in both structures to show the delocalization of
electron pairs. Include lone pairs of electrons, formal charges,
and hydrogen atoms.
Draw a major resonance structure for the following enolate. Use curved arrows in both structures to show the delocalization of electron pairs. Include lone pairs of electrons, formal charges, and hydrogen atoms.
3 (15 marks). Draw a reasonable mechanism that accounts for the formation of the unexpected product shown below. Use curved arrows to show the movement of electrons and show the structures of all intermediates. Do not draw the structures of transition states. Do not include stereochemistry. Be sure to include formal charges and lone pairs of electrons where appropriate. OH HCI ether
Below is the SN1 reaction of
(S)-2-iodopentane and bromide (Br–). Complete
the mechanism by providing the missing curved arrow notation, lone
pairs of electrons, and nonzero formal charges. Be sure to draw the
two organic products that will be produced in the third box.
16 Question (3 points) @ See page 407 Below is the Sn1 reaction of (9)-2-iodopentane and bromide (Br). Complete the mechanism by providing the missing curved arrow notation, lone pairs of electrons, and nonzero formal charges....
07 Question (3 points) Below is the E1 reaction between t-butyl chloride and water (H20). Draw the missing curved arrow notation in the first and second boxes to reflect electron movements. In all boxes, add lone pairs of electrons and nonzero formal charges. 1st attempt See Periodic Table See Hint HAKA Draw the missing curved arrow notation. Add lone pairs of electrons and nonzero formal charges.
NaBH4, ETOH olyto bom. Of= (stereochemistry intentionally omitted) (optically active) A. Draw a mechanism using curved arrow notation for the formation of the product in the reaction above. Make sure to include all relevant lone pairs, bonds, and formal charges. (8 pts)
Peroxyacids (RCO3H) can convert alkenes into epoxides. Draw the two products and the mechanism arrows for the following reaction. Be sure to include lone pairs of electrons and nonzero formal charges on all species. 1st attempt See Periodic Table See Hint Draw curved arrow notation to show the reaction between the peroxy acid and the alkene.