Draw the mechanism and the energy diagram for the reaction shown below. Include any resonance structures for the intermediates of the reaction. H3O+
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- For the following reaction there are three (3) possible products. Two of the products are expected to be minor and one product is expected to be a major product. Br H₂O Name and draw out the step-by-step mechanisms by which each of the products is formed. Briefly explain why one of the three products is expected to be a major product.Part IV: Draw the mechanism and the energy diagram for the reaction shown below. Include any resonance structures for the intermediates of the reaction. Br A OHConsider this reaction: Br CH;OH Br-Br H3CO The mechanism proceeds through a first cationic intermediate, intermediate 1. Nucleophilic attack leads to intermediate 2, which goes on to form the final product. In cases that involve a negatively charged nucleophile, the attack of the nucleophile leads directly to the product. Br + CH3OH Br Intermediate 1 Intermediate 2 (product) In a similar fashion, draw intermediate 1 and intermediate 2 (final product) for the following reaction. OH + Br2 + HBr Br racemic mixture
- didentify the Allowry reactions, as substitution, elimination, or addition DrawWelection arrows to show how the in each reactors Circle and identify any reactive bands break & form intermediates of carbon. Ħ Br Br → AH-Br →→ → XB²Predict the product of the following organic reaction: CH₂ CH O || C–CH2–CH=CH—(CH2)3 CH3 (CH₂)3 CH=CH- - CH₂ CH3 + 4 H₂ Ni CH,−O -C–CH2–CH=CH–CH=CH–CH2–CH3 Specifically, in the drawing area below, draw the chemical structure of the product P. If there is no product, because this reaction won't happen, check the No reaction box under the drawing area. Click and drag to start drawing a structure. × Ś +Determine the major thermodynamic and kinetic products in the following reaction. Br₂
- Chemistry HO -OEt HCI (catalytic) H₂O + EtOH Draw the arc arrow mechanism. Include all relevant free electron pairs, arc arrows, formal charges, structures of intermediates and by-products. Hint: the reaction starts with the protonation of alcoholThere are two mechanisms by which each of the C1 atoms in the following molecule can be replaced by another group: ⚫ Mechanism 1: The C1 atom can be replaced with a concerted, bimolecular step. Mechanism 2: The C1 atom can be replaced in several steps, the slowest of which is unimolecular. Highlight in red the C1 atom that would be replaced the fastest if the reaction went Mechanism 1. Highlight in blue the C1 atom that would be replaced the fastest if the reaction went Mechanism 2. If you would choose the same C1 to be replaced fastest by both mechanisms, highlight it in green instead. C1 cl. C14. Outline a detailed mechanism for the reaction below. Identify the abbreviation for the reaction mechanism. НО H3PO4
- Which SN2 reaction will occur most rapidly? (Assume the concentrations and temperatures are all the same.) * CH;0 CH3 CI + CI CH,0 + CH + I CH3 C CH;O¯ + + F CH D CH,O Br + BrDraw the energy diagram of the following reaction (label and draw reactants, intermediates, and products). Label transition state of the rate limiting step and draw the transition state of the rate determining step. Is it a concerted or stepwise reaction? Write the rate law for this reaction. How do we increase the reaction rate? If we use deutrium-tert-butyl bromide such as (CD3)3CBr instead of (CH3)3CBr, will it increase or decrease the reaction rate? Or there is no meaningful rate change. Write reasons for your answer. Draw mechanisms for reactions by drawing arrows and intermediates.Write a mechanism for this reaction: Br Br₂ H2O + ОН Br OH
