Show mechanism using arrows of reaction NaCIO + 2Nal +2CH CO2H12 + NaCI + H20+ 2 CH3CO2Na 2s20,2 +I2 (brown) S,0%2 (colourless) NaCIO + 2Nal +2CH CO2H12 + NaCI + H20+ 2 CH3CO2Na 2s20,2 +I2 (b...
For the mechanism, show all the steps with multiple reaction
arrows, electron arrows, formal charges, etc.
CONCEPT QUESTIONS Predict the Product. Provide the stable organic product(s) for the reactions below. 1. Mgº, CH3CH2OCH,CH3 2. CO2 (g) 3. H20, HCI 1. MgBr (1eq.) 2. H20, HCI Mechanism. Using ChemDraw, provide the complete mechanism for the following transformation. You must include appropriate arrows, intermediates, and formal charges. 1. MgCI 2. H20, HCI
Write a mechanism for the reaction using curved arrows to show electron reorganization. Write a mechanism for the reaction using curved arrows to show electron reorganization. Consult the arrow-pushing instructions for the convention on regiospecific electrophilic attack on a double bond.
Please show full mechanism with arrows and mechanism
name used in each step. Show all product(s).
Me Nal Me Naci DMF Me HCI Me он НІ DMF
please show mechanism for each step with arrows
1) BH3 2) H2O2, NaOH, H20
2) Draw a rational mechanism for the reaction shown below. Use curved arrows appropriately. Show all relevant intermediate(s) and lone pairs of electrons and formal charges where appropriate. Show ALL STEPS (i.e Reaction 2) 1) Na O Et, EtOH Et 2) H20, HCI Et
2. Show the mechanism by drawing all arrows, charges, and major product(s) that result Remember to show any tautomerization where necessary. (3 points) Cl2 (a) excess (b) M H2SO4 HgSO4, H20
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Show the complete mechanism for the reaction of trans-2-butene with Br using curved arrows to represent every bond broken and every bond formed Pay careful attention to the stereochemistry, using dashes and wedges to draw the reactant, intermediate, and product. Name the product or products. Be sure to include the stereochemical configuration of the product(s) if necessary. Part 4. Synthesis (5 points each). Show a reasonable synthetic pathway for the following transformations, 1. Acetylene - 1,2-butanediol 2. cis-2-butene-trans-2-butene
Write a mechanism for the reaction using curved arrows to show electron reorganization. Consult the arrow-pushing instructions for the convention on regiospecific electrophilic attack on a double bond.
(3) [12 points] Present a detailed mechanism for this reaction. Use curved arrows to show the motion of electrons. You may use the symbol “+ H" and "taut" above reaction arrows to represent a protonation-deprotonation sequence and a tautomerization, respectively. هر) + H20 + H H
also show the mechanism and curved arrows for each
mechanism
2. Predict the products for the reaction between le products for the reaction between Br, as well as Br/H, and the Alkenes listed below. rredict whether each reaction is syn- or anti-, Label the substrate, nucleophile and electrophile in each reaction. Substrate Structure Overall Reaction with Brz (with products) syn- or Overall Reaction with Bry/H20 (with products) anti- 3,3-dimethyl-1-1 butene 1-hexene styrene (phenylethene)