(UPLOAD THIS PAGE TO SHOW YOUR WORK) 6. Haloalkane RXN mechanisms. Please draw an arrow pushing...
s. Using arrow-pushing mechanisms, write the expected products from the following reactions and indicate whether the equilibrium lies to the "right or to the "left". Very briefly explain your reasoning. If resonance is important, show this. If given pKa values calculate Keq. (X pts) d.
s. Using arrow-pushing mechanisms, write the expected products from the following reactions and indicate whether the equilibrium lies to the "right or to the "left". Very briefly explain your reasoning. If resonance is important, show...
Please show your arrow pushing mechanisms for the two
products I request below.
I am trying to check if I did this problem
correctly.
Draw the complete arrow pushing mechanism for the following reaction produc o fierstep! ulo Nucleophile CI-CI did 2 clau produd after er Step D Apr eBo tease show mechanism for
Predict the Major product(s) for the following reactions and draw their corresponding arrow-pushing mechanisms. If there is no reaction write NR. (21 points total) detailed Show the correct stereochemistry when needed KOH THF substitution Cl Mechanism: MeOH substitution Mechanism: CI t-BuOK, DMF heat elimination Mechanism:
please show reaction arrow pushing mechanisms and products of
each. each proceeds via SN1 reaction
oH 7r+ AOH b) c) 7er t 1
please show reaction arrow pushing mechanisms and products of
each. each proceeds via SN2 reaction
Br Nax b) Br NaI +8r NaI c)
please show all arrow pushing mechanisms and the products of
the reactions
он Na I 6) Mor & NaI
The following reaction follow an E1 mechanism. Propose an arrow-pushing mechanism for the following transformations using proper curved arrows: Conc. H2SO4 heat By what mechanisms are the following reactions likely to occur? Draw the major product(s) for each reaction. Show relevant stereochemistry if appropriate. If the expected products are racemic, just draw one enantiomer and write racemic. NaoMe NaoMe OTS NaSH OTS H20
b 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. Arrow-pushing Instructions inox tv no H- B Draw the organic product of the following reaction. CH3 meta-Chloroperoxy- benzoic acid • You do not have to consider stereochemistry. • Indicate regiochemistry when relevant. • The aromatic ring, when present, is unreactive in all cases. • Do not draw organic or inorganic by-products....
Chem 306 Unit 2 Exam Page 5 of 6 7. Draw a reasonable arrow-pushing mechanism to show how the reactant transformed into the final products: (First arrow shown: 14 pts if all correct) Products Reactants 0 + H₂O он (cat.) HO 0 + H₂O H-0 + Ho H . H 1 0 o Hº 0 H 8. a) Consider the polymer below. Circle all reasonable reactants that can be used to make the indicated polymer A. (8 pts) Possible monomers...
Draw curved arrows to show electron reorganization for the reaction step below ts 2req Visted Arrow-pushing Instructions CXm pts pts 2req HO: н 1 pls н о н C=c-H H-: C-C-H Н + + H Н Draw curved arrows to show electron reorganization for the reaction step below. 1 pts 2req w Arrow-pushing Instructions Show.1 pts 1 pls 2req on 1 pls H H H H H EkUView opIca Kelerences Noting the curved arrows, draw all the product(s), organic and...