
Concept explainers
(a)
Interpretation:
Chemical equation that shows reactants, product and catalyst needed for the reaction of propene with chlorine based on Markovnikov’s rule has to be written.
Concept Introduction:
In this reaction no atoms or group of atoms are removed. Instead the unsaturated bond is reduced to saturated bond. A general scheme for addition reaction of
Halogenation reaction is an example of addition reaction. In this reaction, the halogen atoms are added across the double bonds. Chlorination and bromination are the most commonly used halogenation reaction. For halogenation reaction, no catalyst is required.
Markovnikov’s rule:
When an unsymmetrical molecule of formula HQ to an unsymmeterical alkene, the hydrogen atom from HQ gets attached to the unsaturated carbon atom which has the most hydrogen atoms. In other words, it can be said that the hydrogen atom gets attached to the unsaturated carbon atom that is least substituted.
(b)
Interpretation:
Chemical equation that shows reactants, product and catalyst needed for the reaction of propene with hydrogen chloride based on Markovnikov’s rule has to be written.
Concept Introduction:
Chemical reaction in which an atom or a group of atoms are added to each carbon atom of a carbon‑carbon multiple bond in a hydrocarbon or hydrocarbon derivative is known as addition reaction.
In this reaction no atoms or group of atoms are removed. Instead the unsaturated bond is reduced to saturated bond. A general scheme for addition reaction of alkene can be given as shown below,
Asymmetrical addition reaction is the one in which two different atoms or group of atoms are substituted across the multiple bond resulting in the formation of product. No catalyst is required for this reaction.
(c)
Interpretation:
Chemical equation that shows reactants, product and catalyst needed for the reaction of propene with hydrogen based on Markovnikov’s rule has to be written.
Concept Introduction:
Chemical reaction in which an atom or a group of atoms are added to each carbon atom of a carbon‑carbon multiple bond in a hydrocarbon or hydrocarbon derivative is known as addition reaction.
In this reaction no atoms or group of atoms are removed. Instead the unsaturated bond is reduced to saturated bond. A general scheme for addition reaction of alkene can be given as shown below,
Hydrogenation is a type of addition reaction. In this reaction, hydrogen atoms are added across the multiple bonds present in organic molecule. In case of alkenes to undergo hydrogenation, heating the alkene with presence of catalyst such as nickel or platinum is required.
(d)
Interpretation:
Chemical equation that shows reactants, product and catalyst needed for the reaction of propene with hydrogen bromide based on Markovnikov’s rule has to be written.
Concept Introduction:
Chemical reaction in which an atom or a group of atoms are added to each carbon atom of a carbon‑carbon multiple bond in a hydrocarbon or hydrocarbon derivative is known as addition reaction.
In this reaction no atoms or group of atoms are removed. Instead the unsaturated bond is reduced to saturated bond. A general scheme for addition reaction of alkene can be given as shown below,
Asymmetrical addition reaction is the one in which two different atoms or group of atoms are substituted across the multiple bond resulting in the formation of product. No catalyst is required for this reaction.

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Chapter 2 Solutions
Organic And Biological Chemistry
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- Show how each of the following transformations might be best accomplished. More than one step may required. Show all reagents and all intermediate structures. [4 only] CH3 A. CH CH2 C Br CH3 CH3 CH3CH2 C NH2 CH3 B OH any source of carbon N MIHarrow_forwardConsider the reaction below to answer the following questions. 0 0 25 PS ES 1919sds-III msx H H + 5% NaOCH 3, CH3OHA O CH₂OH Jeiniog 2E1 gniwool of mor]. Ignibuloni 9vil 19 A B 11 >buoqm gniwollol so dass 101 tomboy boo-11Coble or to r ton auch i viw ninlaxs, noitsausbroo 152 lobla ogsbau ton 250b br A. Which carbonyl compound functions as the electrophile in this reaction? B. Draw the structure of the enolate ion that is generated during the course of this reaction. C. This reaction is an example of: a. a mixed Claisen condensation. b. C. d. a Dieckman condensation. a Michael reaction. a mixed aldol reaction. HD HDarrow_forwardConsider the reaction below to answer the following questions: 847 Acetoacetic ester can be prepared by the Claisen self-condensation reaction of ethyl acetate. H₁C 0 H 0 IL 유 || OCH2CH3 1. NaOEt, EtOH C 2. H₂O H3C CH₂ Cold not tobizmo. S OCH2CH3 A. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and draw all intermediate structures. B. Ethyl acetate can be prepared from ethanol as the only organic starting material. Show all reagents and structures for all intermediates in this preparation. C. Give the structures of the ester precursors for the following Claisen condensation product and formulate the reaction. ou OELarrow_forward
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- . Each of the following compounds can be prepared by a mixed aldol condensation reaction. Give the Cructures of the aldehyde and/or ketone precursors for each aldol product and formulate the reaction. 0 CH=CHCCH 3. Ph 1arrow_forward. Consider the reaction below to answer the following question: H NaOEt H BOH بلی H + H₂O A. Write the complete stepwise mechanism for the reaction above. Show all intermediate structures and all electron flow with arrows. B. This reaction is an example of: an intramolecular aldol condensation a. an intramolecular Claisen condensation b. C. d. a Robinson annulation a Michael reaction C. The product of this reaction is: a. b. C. d. a ẞ. y-unsaturated aldehyde an a, B-unsaturated ketone an a, B-unsaturated aldehyde an enolarrow_forwardClassify each of the following nitrogen atoms in the following compounds as primary, secondary, tiary, or quaternary. A. B. C. CH3 HO-CHCHNHCH3 ephedrine CH CHCH3 amphetamine NH₂ D. CF H3C CH3 mapiquat chloride HO fexofenadine OH H3C CH3 CO₂Harrow_forward
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