(a)
Interpretation:
A curve-arrow mechanism for the given reaction is to be drawn.
Concept introduction:
The nucleophilic substitution reactions are the reactions in which one nucleophile is substituted by another nucleophile. These reactions depend upon the nucleophilicity and concentration of the nucleophile. There are two types of nuclephilic substitution reaction.
The
(b)
Interpretation:
A curve-arrow mechanism for the given reaction is to be drawn.
Concept introduction:
The reactions in which two substances are combined to give the products is known as addition reaction. The
(c)
Interpretation:
A curve-arrow mechanism for the given reaction is to be drawn.
Concept introduction:
The
(d)
Interpretation:
A curve-arrow mechanism for the given reaction is to be drawn.
Concept introduction:
The chemical reactions in which one molecules combines with the another molecule is known as addition reaction. The polymerization is also a type of addition reaction. The addition of molecules, electrophile or nucleophile to the alkene rings is also a type of addition reaction.
(e)
Interpretation:
A curve-arrow mechanism for the given reaction is to be drawn.
Concept introduction:
A chemical reaction which involves free radicals is known as free radical reaction. These reactions are comprised of three steps, the chain initiation step, the chain propagation step and the last, the chain termination step. The polymerization reactions are a type of free radical reactions.
The free radicals are generated by the hemolytic cleavage of the bond between the atoms and such atoms shares same electronegativity value.
(f)
Interpretation:
A curve-arrow mechanism for the given reaction is to be drawn.
Concept introduction:
A chemical reaction which involves free radicals is known as free radical reaction. These reactions are comprised of three steps, the chain initiation step, the chain propogation step and the last, the chain termination step. The polymerization reactions are a type of free radical reactions. The free radicals are generated by the hemolytic cleavage of the bond between the atoms and such atoms shares same electronegativity value
(g)
Interpretation:
A curve-arrow mechanism for the given reaction is to be drawn.
Concept introduction:
A chemical reaction which involves free radicals is known as free radical reaction. These reactions are comprised of three steps, the chain initiation step, the chain propagation step and the last, the chain termination step. The polymerization reactions are a type of free radical reactions.
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Chapter 5 Solutions
Organic Chemistry
- 19.78 Write the products of the following sequences of reactions. Refer to your reaction road- maps to see how the combined reactions allow you to "navigate" between the different functional groups. Note that you will need your old Chapters 6-11 and Chapters 15-18 roadmaps along with your new Chapter 19 roadmap for these. (a) 1. BHS 2. H₂O₂ 3. H₂CrO4 4. SOCI₂ (b) 1. Cl₂/hv 2. KOLBU 3. H₂O, catalytic H₂SO4 4. H₂CrO4 Reaction Roadmap An alkene 5. EtOH 6.0.5 Equiv. NaOEt/EtOH 7. Mild H₂O An alkane 1.0 2. (CH3)₂S 3. H₂CrO (d) (c) 4. Excess EtOH, catalytic H₂SO OH 4. Mild H₂O* 5.0.5 Equiv. NaOEt/EtOH An alkene 6. Mild H₂O* A carboxylic acid 7. Mild H₂O* 1. SOC₁₂ 2. EtOH 3.0.5 Equiv. NaOEt/E:OH 5.1.0 Equiv. NaOEt 6. NH₂ (e) 1. 0.5 Equiv. NaOEt/EtOH 2. Mild H₂O* Br (f) i H An aldehyde 1. Catalytic NaOE/EtOH 2. H₂O*, heat 3. (CH,CH₂)₂Culi 4. Mild H₂O* 5.1.0 Equiv. LDA Br An ester 4. NaOH, H₂O 5. Mild H₂O* 6. Heat 7. MgBr 8. Mild H₂O* 7. Mild H₂O+arrow_forwardLi+ is a hard acid. With this in mind, which if the following compounds should be most soluble in water? Group of answer choices LiBr LiI LiF LiClarrow_forwardQ4: Write organic product(s) of the following reactions and show the curved-arrow mechanism of the reactions. Br MeOH OSO2CH3 MeOHarrow_forward
- Provide the correct IUPAC name for the compound shown here. Reset cis- 5- trans- ☑ 4-6- 2- 1- 3- di iso tert- tri cyclo sec- oct but hept prop hex pent yl yne ene anearrow_forwardQ6: Predict the major product(s) for the following reactions. Note the mechanism (SN1, SN2, E1 or E2) the reaction proceeds through. If no reaction takes place, indicate why. Pay attention to stereochemistry. NaCN DMF Br σ Ilm... Br H Br H H NaCN CH3OH KOtBu tBuOH NaBr H₂O LDA Et2O (CH3)2CHOH KCN DMSO NaOH H₂O, A LDA LDA Systemarrow_forwardQ7: For the following reactions, indicate the reaction conditions that would provide the indicated product in a high yield. Note the major reaction pathway that would take place (SN1, SN2, E1, or E2) Note: There may be other products that are not shown. There maybe more than one plausible pathway. Br H3C OH H3C CI ... H3C SCH2CH3 CI i SCH2CH3 ཨ་ Br System Settarrow_forward
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- 19. (3 pts) in Chapter 7 we will see a reaction of halocyclohexanes that requires that the halogen occupy an axial position with this in mind, would you expect cis-1-bromo-3-methylcyclohexane or trans-1-bromo-3-methylcyclohexane to be more reactive in this reaction? Briefly explain your choice using structures to support your answer. Mere-eries-cecleone) The tran-i-browse-3-methylcyclohexionearrow_forwardPlease help me calculate the undiluted samples ppm concentration. My calculations were 280.11 ppm. Please see if I did my math correctly using the following standard curve. Link: https://mnscu-my.sharepoint.com/:x:/g/personal/vi2163ss_go_minnstate_edu/EVSJL_W0qrxMkUjK2J3xMUEBHDu0UM1vPKQ-bc9HTcYXDQ?e=hVuPC4arrow_forwardProvide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) H₁₂C C(CH3)3 C=C H3C CH3 CH3CH2CH CI CH3 Submit Answer Retry Entire Group 2 more group attempts remaining Previous Nextarrow_forward
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