a. Label the reactive features of the following reactants, select the most reactive feature, then write and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion will start to develop, and/or if aromatic character will be lost as a result of a reaction between these molecules. benzenesulfonic acid + Cl; and FeCl, b. Use mechanism arrows to illustrate the reaction that occurs.
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- a. Label the reactive features of the following reactants, select the most reactive feature, then write and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion will start to develop, and/or if aromatic character will be lost as a result of a reaction between these molecules. bromobenzene + 2-chloro-3-methyl butane + AICI3 b. Use mechanism arrows to illustrate the reaction that occurs. If applicable, use stabilization resources to deal with the carbocation, carbon radical, or carbanion that starts to develop during the reaction, and draw the structure of any resonance- stabilized intermediate. Continue labelling and diagramming the reaction until you find the major stable product(s). Finally, state the stereochemistry of the major product(s) and use either Fisher projection or perspective formula representations to illustrate that stereochemistry.Organic Chemistry question; Please provide a well explained and correct answer for the following. In Williamson ether synthesis reaction, NaH plays both roles as base and deprotonation to alcohol. How about other chemicals, and can they play the same role ? For instance, 1. Regular strong base, e.g. NaOH, KOH 2. Salt of strong base, weak acid, e.g. CH3COONa 3. Halide acid, e.g. HCl, HBr, HI 4. Salt of alcohol, e.g. CH3ONaShow full curly arrow mechanims and talk about regioselctivity/stereoselctivity. Also, define which one is nucleophile, electrophile, base/acid/reducing agent and reaction name. Thank you
- Label the reactive features of the following reactants, select the most reactive feature, thenwrite and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion willstart to develop, and/or if aromatic character will be lost as a result of a reaction between thesemolecules. bromobenzene + 2-chloro-3-methyl butane + AlCl3If there are unshared pairs of electrons on the atoms directly attached to the aromatic ring, they are the groups that provide electrons to the ring with the effect of ……………… and are ………………… directive towards electrophiles. Groups that are double bonded to a more electronegative atom than the atoms directly attached to the ring are ……… steers that withdraw electrons from the ring with the effect of .................. Groups whose electronegativity is higher than the sp2 carbon of the ring directly attached to the ring will withdraw electrons from the ring as ............. and ……… they are routers. Halogens, on the other hand, withdraw electrons from the ring as ………......... due to their high electronegativity and are ……….. directing. A. Resonance/(o-, p-)/ resonance/(m-)/ inductive/(o-, p-)/ inductive/(o-, p-) B. Resonance/(o-, p-)/ resonance/(m-)/ inductive/(o-, p-)/ inductive/(m-) C. Resonance/(o-, p-)/ resonance/(m-)/ inductive/(m-)/ inductive/(o-, p-) D. Inductive/(o-, p-)/…17. a. Label the reactive features of the following reactants, select the most reactive feature, then write and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion will start to develop, and/or if aromatic character will be lost as a result of a reaction between these molecules. HN-C -CH3 with Cl, and FeCl, b. Use mechanism arrows to illustrate the reaction that occurs. If applicable, use stabilization resources to deal with the carbocation, carbon radical, or carbanion that starts to develop during the reaction, and draw the structure of any resonance- stabilized intermediate. Continue labelling and diagramming the reaction until you find the major stable product(s). Finally, state the stereochemistry of the major product(s) and use either Fisher projection or perspective formula representations to illustrate that stereochemistry.
- The above reaction involves heterolytic bond breakage of HBr a) Encircle the nucleophile (s) and electrophile (s) and explain why. b) Give the mechanism of the reaction by: ) Drawing the appropriate arrows to track the flow of electrons in Showing the species formed after bond breakage and bond formation with appropriate charges. c) Predict the final products.Draw the mechanism showing the Brønsted acid/base reaction between propanoic acid and methylamine. Label the acid, base, conjugate base, and conjugate acid. Show all curved arrows, lone pairs and nonzero formal charges. einedoelM HO, CH;NH, propanoic acid pKa = 4.9 methylamine Mechanism: Using the pKa information provided/pKa tables (table appended to the end of this document), determine whether the starting reagents (propanoic acid and methyl amine) or resulting products would be favored at equilibrium (no math needed!).Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic steps. Be sure to account for all bond-breaking and bond-making steps. **Y...= Select to Add Arrows HCI :CI:O Select to Add Arrows Hội H 19: Draw the product of the reaction shown below. Ignore inorganic byproducts. SH NaH, PhCH₂Cl DMSO Problem 35 of 20 Q Please select a drawing or reagent from the question area Problem 35 of 20 Please select a drawing or reagent from the question area Problem 42 of 20 Submit Atoms, Bonds and Rings Draw or tap a new bond to see suggestions. Charges Submit Undo Remove Reset Done Submit Drag To Pan
- If there are unshared pairs of electrons on the atoms directly attached to the aromatic ring, they are the groups that provide electrons to the ring with the effect of ……………… and are ……………………… directed towards electrophiles. Groups that are double bonded to a more electronegative atom than the atoms directly attached to the ring are ……… guides that withdraw electrons from the ring with the effect of .................. Groups whose electronegativity is higher than the sp2 carbon of the ring directly attached to the ring will withdraw electrons from the ring as ............. and ……… they are routers. Halogens, on the other hand, withdraw electrons from the ring as ………......... due to their high electronegativity and are ……….. directing A. Resonance/(o-, p-)/resonance/(m-)/ inductive/(o-, p-)/ inductive/(o-, p-) B. Resonance/(o-, p-)/resonance/(m-)/ inductive/(m-)/ inductive/(o-, p-) C. Resonance/(o-, p-)/resonance/(m-)/ inductive/(o-, p-)/ inductive/(m-) D. Inductive/(o-,…Methylating agents are substrates that deliver methyl groups to nucleophiles, and so are themselves electrophilic. What is the most common methylating agent (a) in the laboratory and (b) in biological systems? Discuss their similarities and differences... Solve it asapComplete the generic mechanism for an electrophilic aromatic substitution (EAS) reaction using E as the electrophile, and show how the sigma complex is resonance stabilized. Use curved arrows to show the mechanism and the conversion between resonance structures. Make sure to add any missing charges. Note the use of a generic base (B) in the last step. Then, label the reaction coordinate diagram for a typical EAS reaction by correctly placing the structures on the diagram. Step 1: add a curved arrow. Select / |||||| Draw CH Rings Groups More Erase slow WE