3. Draw the major product in the following reaction and reaction mechanism. Remember when drawing a reaction mechanism, you need to show all nonbonding electron pairs, formal charges, electron flow arrows, and all resonance structures. What is the name of this mechanism? Determine and circle whether the substituent is an activator or deactivator. Explain what is meant by being an activator or deactivator and circle the single resonance structure that supports your decision regarding the substituent in the starting material. OH CH₂CH₂CH₂Br FeBra

Determine which mechanism below is the most correct. Be sure to look at whether the most acidic H is reacting, if the direction of the arrows are correct, and if the correct products are formed based on the mechanism. If the correct answer is Option B, then explain why the other options are incorrect?

2. Draw a mechanism for the reaction of the nucleophile and the electrophile as indicated below. Also draw the product produced. CH3 H3C+CI CH3 + HO

3. The haloalkane below is heated in a solution of ethanol and undergoes SN1 and E1S a) Draw the first step of the mechanism of the reaction. b) Show all the more stable carbocations that could be formed from (a). c) Draw all the El products that can be formed from (b). d) Circle the most favorable product(s) and explain your reasoning. e) Name: the most favored product(s).(Note: for cyclic alkenes the carbons of the C-C must be numbered 1,2 and in the name there is no need to specify its position). Br

draw products

Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.

3) Any compound or ion with at least one lone pair can be considered a base and/or a nucleophile. The relative basicity and nucleophilicity of the species is one of the most important factors that determine the mechanism of a reaction on sp³-carbon atoms. Please show an example of a) a reagent that is a strong nucleophile and a strong base, b) a reagent that is a weak nucleophile and a strong base, c) a reagent that is a strong nucleophile and a weak base, d) a reagent that is a weak nucleophile and a weak base. Which nitrogen atom in the structure below is most nucleophilic? Please explain by discussing the electron density around each nitrogen atom. Show at least three resonance structures of the compound. N.

Curved arrows are used to illustrate the flow of electrons. Using the provided starting structure, 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. Then draw the organic product of this reaction. Include all lone pairs in the structures. Ignore inorganic byproducts, counterions, and solvents. Incorrect, 2 attempts remaining H & H H Select to Add Arrows H₂O heat H :O: :Br: H H Select to Add Arrows H₂O heat Select to Draw Product

Can you assist me in spotting my error in drawing out this mechanism? I understand that it's an SN1 reaction and can't figure out why the the drawing is incorrect. Thank you very much.   Original Question: Draw the mechanism for the following reaction: Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron-flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created.

(in first pic) need help with the last one, with the alkyne & the question in the 2nd pic.  thank you!!