(a)
Interpretation: Major products for the given set of reactions have to be found.
Concept Introduction:
The nitro group present in the compound is reduced to amino group by using Fe, Zn, Sn or SnCl2 in the presence of aqueous acid followed by the treatment with base such as NaOH. This reaction is more mild approach. It can be carried out in the presence of the other
To find: Using a reduction followed by base treatment, prepare the major product of (a)
Find the reaction of the starting material of (a) with Fe, H3O+
(b)
Interpretation: Major products for the given set of reactions have to be found.
Concept Introduction:
Sodium cyanoborohydride is a strong reducing agent than sodium borohydride. It reduces the carbonyl group into amine group in a rapid way. So, it is called as reductive amination reactions.
Aldehyde or ketone group is reacted with primary amine in the presence of sodium cyanoborohydride as a reducing agent and a proton source in the reaction medium to produce secondary amines.
Aldehyde or ketone group is reacted with secondary amine in the presence of sodium cyanoborohydride as a reducing agent and a proton source in the reaction medium to produce tertiary amines.
To find: Using a reductive amination, prepare the major product of (b)
Decide the reaction and the nature of the product
(c)
Interpretation: Major products for the given set of reactions have to be found.
Concept introduction:
The reduction of lithium aluminum hydride on nitriles followed by water work-up gives amine with an additional carbon atom in their chain. This type of reaction is applied to increase the carbon skeleton and change in the identity of the functional group.
To find: The major product of the reaction (c)
Give for the formation of lithium salt by reduction
(d)
Interpretation: Major products for the given set of reactions have to be found.
Concept introduction:
The reduction of lithium aluminum hydride on nitriles followed by water work-up gives amine with an additional carbon atom in their chain. This type of reaction is applied to increase the carbon skeleton and change in the identity of the functional group.
To find: The major product of the reaction (d)
Give for the formation of lithium ion by reduction
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Chapter 22 Solutions
ORGANIC CHEMISTRYPKGDRL+MLCRL MDL
- Predict the major organic product(s), if any, of the following reactions. Assume all reagents are in excess unless otherwise indicated.arrow_forwardHow many signals would you expect to find in the 1 H NMR spectrum of each given compound? Part 1 of 2 2 Part 2 of 2 HO 5 ☑ Х IIIIII***** §arrow_forwardA carbonyl compound has a molecular ion with a m/z of 86. The mass spectra of this compound also has a base peak with a m/z of 57. Draw the correct structure of this molecule. Drawingarrow_forward
- Can you draw this using Lewis dot structures and full structures in the same way they are so that I can better visualize them and then determine resonance?arrow_forwardSynthesize the following compound from cyclohexanol, ethanol, and any other needed reagentsarrow_forwardFor a titration of 20.00 mL of 0.0500 M H2SO4 with 0.100 M KOH, calculate the pH at each of the following volume of KOH used in the titration: 1) before the titration begin; 2) 10.00 mL; 3) 20.00 mL; 4) 30.00 mL. Ka2 = 1.20×10-2 for H2SO4.arrow_forward
- Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s) Be sure to account for all bond-breaking and bond-making steps Problem 73 of 10 Drawing Amows ro HO Donearrow_forward12. Synthesize the following target molecules (TMs) using the specified starting materials. .CI a) HO3S SM TM b) HO- SMarrow_forwardFor a titration of 20.00 mL of 0.0500 M H2SO4 with 0.100 M KOH, calculate the pH at each of the following volume of KOH used in the titration: 1) before the titration begin; 2) 10.00 mL; 3) 20.00 mL; 4) 30.00 mL. Ka2 = 1.20×10-2 for H2SO4.arrow_forward
- Write the systematic name of each organic molecule: structure name show work. don't give Ai generated solutionarrow_forwardShow work with explanation needed. Don't give Ai generated solutionarrow_forwardA Elschboard Part of SpeechT-D Alt Leaming App app.aktiv.com Curved arrows are used to illustrate the flow of electrons. Using the provided resonance structures, draw the curved electron- pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond-breaking and bond-making steps. Include all lone pairs and formal charges in the structures. Problem 45 of 10 I Select to Add Arrows N Please selarrow_forward
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