(a)
Interpretation:
The intermediate (A) formed by the reactants has to be identified. The mechanism for the formation of intermediate has to be shown.
Concept introduction:
Base abstracts an acidic proton to form a negatively charged species. The negative charged species is called nucleophile. The carbon which is attached to the electronegative atom is called the electrophilic carbon.
In the
(b)
Interpretation:
The mechanism for the conversion of A to B has to be shown. The compound which formed more rapidly has to be identified.
Concept introduction:
The reaction which takes place between two or more than two atoms which are present in the same molecule are called the intramolecular reactions.
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EBK ORGANIC CHEMISTRY
- Compound A reacts with B in the presence of sodium hydride to give C as the majority product.1. Give the detailed mechanism of the formation of C and draw the product C in the box above.2. Draw the energy diagram of the reaction. Indicate with an arrow the rate-determining step of the reaction then draw its transition state3.The rate of the reaction observed is 5 x 10-2 M.s-1 when the concentrations of A and B are 0.2 M and 0.1 M respectively.Determine the rate of the reaction if the concentrations of A and B are now 0.3 M and 0.2 M respectively. Show your calculationarrow_forwardA synthetic chemist at ALEKeneS Industries, a little known hydrocarbon production plant, performed the following reaction, and collected the alkene products (any others were discarded). Br A major major The chemist remembered to write down the starting material, and that two major products were collected, but forgot to write down the identity of reagent A. Decide if any of the following reagents are a good candidate for A, as well as the mostly likely mechanism for the reaction. Explanation Reagent Is this a good candidate for reageant A? :N DBU Z: HO-CH3 :OH Yes, using an E1 mechanism Yes, using an E2 mechanism No, not a good candidate for this reaction Yes, using an E1 mechanism Yes, using an E2 mechanism ONo, not a good candidate for this reaction Yes, using an E1 mechanism Yes, using an E2 mechanism ONo, not a good candidate for this reaction Check ? ollo 18 Ar © 2024 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forward3,) you have now eliminated one substitution site and should have two possible sites remaining. Provide a mechanism for the formation of each of the two remaining products. You should include all possible. Resident structures for the cat on intermediates. There should be four resident structures in each mechanism. You do not need to show the mechanism for the formation of the electrify you may assume that only a single iodine will add to the ring. a. b. GOLDEST GAD SE 1029 OH H OH 02AB o 1o1 meiasdoorn woms bevis song of olds pel I+ noboibong tombong 10 to asiqisminoviowTill bris H₂O, EtOH naut nobibba as gada tasest 30 no odt to toubong Input sdr lo notaxillaryn I+ bouborg on to ving di salmsibb or O etshqoqs edt onimaob or atob MM O bax H seu zie.baz anoitecu dale19 H₂O, EtOH lliw gan snated a no quorg lanoituut invellib.noimadue shamore siliqotools al Hoib blaos tad aquosy Insoitonut oor za milline V.mobest ad not sila noistade sitt lenoiraut dues bleno) nobedog ad to goitool…arrow_forward
- A. Provide a reasonable mechanism for the non-enzymatic transformation shown below. H H+ + H₂Oarrow_forwardJj.29.arrow_forward4. Provide the complete mechanism using Curved Arrow Formalism for the compound shown below treated with H2SO4/H2O. Include all resonance stabilized intermediates. Tell which layer (aqueous or organic) the product(s) will be isolated in. HO. N.arrow_forward
- V. In the following reaction: CH3CH₂Br + CH3COOK → CH3COOCH₂CH3 +KBr Adding a small amount of sodium iodide increases the reaction rate significantly. Please using the reaction mechanisms, nucleophilicity and leaving group quality to explain.arrow_forwardMelphalan, a drug used in chemotherapy, reacts with itself in the body before binding with its target, as illustrated in the mechanism below. What is the first pattern of arrow pushing seen in this reaction? (Look at the first arrow coming from the Nitrogen with a lone pair). a. rearrangementc. nucleophilic attackarrow_forwardGive good explanation with hand written solution Plzarrow_forward
- Compound A is heated with methanol B to give product C.has. Give the majority product C and draw the mechanism of its formation. Indicate with an arrow the determining step of the rate of this reaction then draw its transition statearrow_forwardComplete the mechanism and draw the final product for the Grignard reaction below. It is not necessary to draw byproducts. .. Br Mg : 0 H. Et, 0 H,O* :* :arrow_forwardDraw ALL possible products (including cis/trans isomers) if the compounds below were to undergo elimination. THEN indicate which will be the major elimination product and briefly explain why. a. d. OTS b. e. Br C. Brarrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning