PLEASE ANSWER ALL A-G, will give thumbs up!! FOR A, just need explanation why reaction occurs at C2 position rather than C3, already have mechanism drawn...
PLEASE EXPLAIN OR AT LEAST JUST ANSWER ALL ASAP, BEFORE TOMORROW!!
PLEASE ANSWER ALL A-G, will give thumbs up!! FOR A, just need explanation why reaction occurs...
show a stepwise mechanism for structure A and B. used curved arrows
to show the flow of electrons as well as lone pairs, charges, and
pertinent resonance structures.
GU AIGI + ΗΝ. cat. H2SO4 H0
Write the complete stepwise mechanism for the
acid catalyzed hydrolysis of the compound shown. Show all
intermediates, indicate with curved arrows the movement of
electrons and show all formal charges and lone pairs of electrons
where relevant. Will rate and comment, thank you in
advance!
i
really need help, please help i will rate thanks
Write the complete stepwise mechanism for the acid catalyzed hydrolysis of the compound shown. Show all intermediates, indicate with curved arrows the movement of electrons and show all formal charges and lone pairs of electrons where relevant
Draw the one-step synthesis for this compound using an
SN2 reaction. Use Br- as leaving group. Add
curved arrow(s) to show moving of electrons in your mechanism.
Include lone pairs and formal charges in your answer. Do not show
metal cation in your mechanism.
x Your answer is incorrect. Try again. Draw the one-step synthesis for this compound using an SN2 reaction. Use Br' as leaving group. Add curved arrow(s) to show moving of electrons in your mechanism. Include lone...
7. Provide a detailed me rovide a detailed mechanism for the following transformation. Be sure to use curved arrows, Show all relevant lone pairs and bonds, formal charges and all intermediates. Be sure to account for the appropriate stereochemistry. (5 points) NaH (1 equiv), THF Me Me
i need steps 3.4,6 please
11. 20/19 23 Question See page 1062 points) Provide the missing curved arrows and structures to complete the mechanism of the Fischer esterification. Your structures should indude all nonzero formal charges and one pairs of electrons. The reagents you need for each mechanistic step are provided in each box. 29th attempt See Periodic Table See Hint op Draw the organic intermediate with lone pair electrons and non-zero formal charges. Add the curved arrow notation.
Hydration of alkenes under aqueous acidic conditions. Draw the detailed stepwise mechanism for this reaction. Be sure to show all steps, intermediates, formal charges, and show the movement of electrons with curved arrows. You do not need to draw transition states. H2SO4 H20 ?? The hydration of alkynes can also occur under aqueous acidic conditions however, instead of forming the alcohol, a ketone is formed. Draw the detailed stepwise mechanism for the conversion of the alkyne to the ketone (one...
10. Provide a detailed mechanism for the following transformation. Be sure to use curved arrows, correct reaction arrows, Show all relevant lone pairs and bonds, formal charges and all intermediates. Think about what your components are and what would happen first. (5 points) HBr Me on me mé Br + Ho Me
just need step 5
25 Question (6 points) See pese 1069 Provide a mechanism for the Dieckmann condensation shown here by providing the missing structures (including the final product) and curved arrows. Your structures should include all nonzero formal charges and lone pairs of electrons. When drawing the enolate, place the negative charge on the carbon not the oxygen. 20th attempt See Periodic Table See Hint the missing curved arrow notation VIEW SOLUTION We were unable to transcribe this image
9. a) Write the detailed Sn1 mechanism for the reaction of (S)-3-bromo-3-methylhexane with H20, showing curved arrows, relevant lone pairs, formal charges, stereochemistry for each step. Include any transition states and/or intermediates, and name the product(s). b) A racemic mixture results from a reaction of the chiral alkylbromide starting material below, and acetate. at hope ܬ Write the complete mechanism for the synthesis. Show the curly arrows, relevant lone pairs and all formal charges for each step. Include any transition...