
(a)
Interpretation:
Structure of amine or quaternary ammonium salt that is obtained when trimethylamine and ethyl bromide is reacted in presence of strong base has to be drawn.
Concept Introduction:
Alkylation reaction is a reaction in which the transfer of alkyl group from one molecule to another molecule takes place. While considering
(a)

Answer to Problem 17.69EP
The structure of product obtained is,
Explanation of Solution
Given reactants are trimethylamine and ethyl bromide. In this, the amine given is a tertiary amine. When tertiary amine is treated with an alkyl halide, the product obtained is a quaternary ammonium salt. The complete reaction and the structure of the product formed is given as,
Structure of the product formed is drawn.
(b)
Interpretation:
Structure of amine or quaternary ammonium salt that is obtained when diisopropylamine and methyl bromide is reacted in presence of strong base has to be drawn.
Concept Introduction:
Alkylation reaction is a reaction in which the transfer of alkyl group from one molecule to another molecule takes place. While considering amines, the alkylating agent that is used is alkyl halides. Alkylation is done under basic conditions. The general equations for amines alkylation process is,
(b)

Answer to Problem 17.69EP
The structure of product obtained is,
Explanation of Solution
Given reactants are diisopropylamine and methyl bromide. In this, the amine given is a secondary amine. When secondary amine is treated with an alkyl halide, the product obtained is a tertiary amine. The complete reaction and the structure of the product formed is given as,
Structure of the product formed is drawn.
(c)
Interpretation:
Structure of amine or quaternary ammonium salt that is obtained when ethylmethylpropylamine and methyl chloride is reacted in presence of strong base has to be drawn.
Concept Introduction:
Alkylation reaction is a reaction in which the transfer of alkyl group from one molecule to another molecule takes place. While considering amines, the alkylating agent that is used is alkyl halides. Alkylation is done under basic conditions. The general equations for amines alkylation process is,
(c)

Answer to Problem 17.69EP
The structure of product obtained is,
Explanation of Solution
Given reactants are ethylmethylpropylamine and methyl chloride. In this, the amine given is a tertiary amine. When tertiary amine is treated with an alkyl halide, the product obtained is a quaternary ammonium salt. The complete reaction and the structure of the product formed is given as,
Structure of the product formed is drawn.
(d)
Interpretation:
Structure of amine or quaternary ammonium salt that is obtained when ethylamine and ethyl chloride is reacted in presence of strong base has to be drawn.
Concept Introduction:
Alkylation reaction is a reaction in which the transfer of alkyl group from one molecule to another molecule takes place. While considering amines, the alkylating agent that is used is alkyl halides. Alkylation is done under basic conditions. The general equations for amines alkylation process is,
(d)

Answer to Problem 17.69EP
The structure of product obtained is,
Explanation of Solution
Given reactants are ethylamine and ethyl chloride. In this, the amine given is a primary amine. When primary amine is treated with an alkyl halide, the product obtained is a secondary amine. The complete reaction and the structure of the product formed is given as,
Structure of the product formed is drawn.
Want to see more full solutions like this?
Chapter 17 Solutions
GENERAL,ORGANIC,+BIO.CHEM.-MINDTAP
- I need help with the followingarrow_forwardFor Raman spectroscopy/imaging, which statement is not true regarding its disadvantages? a) Limited spatial resolution. b) Short integration time. c) A one-dimensional technique. d) Weak signal, only 1 in 108 incident photons is Raman scattered. e) Fluorescence interference.arrow_forwardUsing a cell of known pathlength b = 1.25115 x 10-3 cm, a water absorption spectrum was measured. The band at 1645 cm-1, assigned to the O-H bending, showed an absorbance, A, of 1.40. a) Assuming that water density is 1.00 g/mL, calculate the water molar concentration c (hint: M= mole/L) b) Calculate the molar absorptivity, a, of the 1645 cm-1 band c) The transmitted light, I, can be written as I= Ioexp(-xb), where x is the absorption coefficient (sometimes designated as alpha), Io is the input light, and b is the cell pathlength. Prove that x= (ln10)*x*c. (Please provide a full derivation of the equation for x from the equation for I). d) Calculate x for the 1645 cm-1 bandarrow_forward
- For CARS, which statement is not true regarding its advantages? a) Contrast signal based on vibrational characteristics, no need for fluorescent tagging. b) Stronger signals than spontaneous Raman. c) Suffers from fluorescence interference, because CARS signal is at high frequency. d) Faster, more efficient imaging for real-time analysis. e) Higher resolution than spontaneous Raman microscopy.arrow_forwardDraw the major product of the Claisen condensation reaction between two molecules of this ester. Ignore inorganic byproducts. Incorrect, 5 attempts remaining 1. NaOCH3/CH3OH 2. Acidic workup Select to Draw O Incorrect, 5 attempts remaining The total number of carbons in the parent chain is incorrect. Review the reaction conditions including starting materials and/or intermediate structures and recount the number of carbon atoms in the parent chain of your structure. OKarrow_forwardUsing a cell of known pathlength b = 1.25115 x 10-3 cm, a water absorption spectrum was measured. The band at 1645 cm-1, assigned to the O-H bending, showed an absorbance, A, of 1.40. a) Assuming that water density is 1.00 g/mL, calculate the water molar concentration c (hint: M= mole/L) b) Calculate the molar absorptivity, a, of the 1645 cm-1 band c) The transmitted light, I, can be written as I= Ioexp(-xb), where x is the absorption coefficient (sometimes designated as alpha), Io is the input light, and b is the cell pathlength. Prove that x= (ln10)*x*c d) Calculate x for the 1645 cm-1 bandarrow_forward
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning





