Nam 1) Show the mechanism usin g curved arrows to show the formation of the products...
1. Use curved arrows to show the mechanisms of formation of the substitution products in each reaction. Indicate stereochemistry of the products where necessary. [10 points] OCH3 DMSO BrH ♡ CH,CH,OH CH3CH2OH Br a Br NaOH NaOH THF
уон 6. The following reaction yields multiple products (16 points) H2O H2SO4 Use curved arrows to show the mechanism for the formation A. Use curved arrows to show the mechanism for the formation B. Use curved arrows to show the mechanism for the formation of C.
For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H, SO2, then draw the structures of the minor and major products of the elimination. H2SO4 - Major and Minor products O Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation of the carbocation intermediate for the elimination. Select Draw Rings More Erase Select Draw...
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)
Use curved arrows to show the mechanisms of formation of the substitution products in each reaction. Indicate stereochemistry of the products where necessary. [10 points] OCH3 а) DMSO Br H CH3CH2ОH b) Br NaOH c) THF
Provide the detailed stepwise mechanism using curved arrows to show electron movement that accounts for the formation of the products shown . НО* ОН COOH
1. Provide the products of the reaction below and a detailed reaction mechanism using curved arrows to indicate the movement of electrons. (a) (b) КОН (c) Note that formation of 4- or 7-membered rings is disfavored. Hiyo KOH acidie workup 2. An interesting problem that involves a bit of review (imines and Grignard chemistry) and application of what you previously learned to a new reaction: The Carbon of an imine functional group (i.e. R.C-NR) is sufficiently electron deficient to be...
Add arrows to the boxes to show the mechanism of the formation of the thermodynamic product of the reaction. All charges, necessary lone pairs, bonds are shown, so you only have to provide the curved arrows to convert a structure to the one in the following box. In the last box, draw the thermodynamic product of the reaction. Include any necessary lone pairs in your structure. **only the second & fourth box is wrong ** please help and explain why....
Show a stepwise mechanism for the following products using curved arrows. 1. Is based on HX additions to alkenes 2. Is based on addition reactions to ketones tox.de HCI VINOH 1. MeMgBr (1 equiv) 2. H30+ OH
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.