Answered: Define the simplest method to…

Science

Chemistry

Define the simplest method to synthesize an amine ?

Chemistry for Today: General, Organic, and Biochemistry

9th Edition

ISBN:9781305960060

Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Chapter16: Amines And Amides

Section: Chapter Questions

Problem 16.27E

See similar textbooks

Related questions

Q: Explain why the boiling point of propanamide, CH3CH2CONH2, is considerably higher than the boiling…

A: Physical properties like boiling point depend upon the molecular mass and intermolecular hydrogen…

Q: W H N. H Classify the following amine. A) primary amine B) secondary amine C) tertiary amine D)…

A: In this question has two parts. In one part : given a structure of a amine Molecule. We have to…

Q: Which of these reagents cannot be used in transforming nitro containing compounds into amines? O…

A: The reagent SnCl2/HCl is a reducing reagent which helps in the reduction of the functional groups.…

Q: Classify each amine in the following compounds as 1°, 2°, or 3°. NH2 a. H,N b. CH,CH20. N-CH,…

A: NH3 is ammonia R-NH2 is primary amine i.e. N attached to one alkyl and two hydrogen atoms forms a…

Q: 2. Draw the structure of the product that will be formed when each of the following amines reacts…

A: When aromatic primary amines means aniline and C-2/C-3/C-4 substituted aniline reacts with NaNO2/HCl…

Q: Draw the structures of the amines from which phenylephrine hydrochloride and methadone hydrochloride…

A: Amines are the derivatives of ammonia, wherein one or more hydrogen atoms of the ammonia have been…

Q: Indicate the following statement as true/false. 1) While ethylamine is soluble in water,…

A: Amines are organic compounds having functional group -NH2.

Q: What amide(s) can be used to prepare each amine by reduction?

A: a.

Q: Predict the products from the reactions of the following amines with sodium nitrite indilute HCl.…

A: Sodium nitrite reacts with HCl to give nitrosonium ion.

Q: Amides do not react with halide ions. Why?

A: Carbonyl substitution reaction is one of the common type of reactions in organic chemistry. In this…

Q: What reactants will product this amide? Draw the reaction

Q: Amines in aqueous solutions are less reactive than amines in gaseous solutions. Select one: O True O…

A: Amines are Lewis’s base due to the presence of a lone pair of electrons on the nitrogen atom of…

Q: What acyl chloride and amine are required to synthesize the following amides?a. N-ethylbutanamide…

A: The preparation amides are done by using carboxylic acids, acyl chlorides and esters. When these…

Q: Draw the structures of the following compounds:) a@aminopropionaldehyde

A: The structure of α-amino propionaldehyde is as follows:

Q: Nor HN N. A OH F There are two nitrogen atoms highlighted and labelled A and B. Match the…

Q: Predict the major products formed when the following amines undergo exhaustivemethylation, treatment…

A: The formation of major product, when the given amine undergoes exhaustive methylation, treatment…

Q: Rank the following amines in order of basicity.

A: The given compounds are: A. B.

Q: Draw a structural formula for each amine and amine derivative. (a) N,N-Dimethylaniline (b)…

A: As per our guidelines we can only solve first three sub-parts of a question. Please resubmit other…

Q: What acids can be used to protonate an amine?

Q: Show how to convert amines to other functional groups, and devise multistepsyntheses using amines as…

Q: be used to prepare following amine by reductive amination? NH2 NH2 NH2 NH2 (III) (IV) (I) (II)

A: Since you have asked multiple question, we will solve the first question for you.If you want any…

Q: Classify the following alkaloid according to the ring system, draw the structure, then give the…

Q: The hydrolysis of an amide in acidic conditions forms A. a carboxylate salt and an alcohol…

A: Given : The hydrolysis of an amide in acidic conditions forms

Q: Predict the major products formed when the following amines undergo exhaustivemethylation, treatment…

Q: * What is the other term for cyclic amides? 33. Liquid amines with higher molecular weight have…

A: Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: neutral because of the polarity are unique as they do not behave like any of the other amines…

A: Basicity is tendency to available lone pair of electrons for an acid.

Q: Which of the following statements is correct regarding aliphatic amines? Select one: O a. aliphatic…

A: The correct statement should be found regarding aliphatic amines.

Q: Explain Formation of Imines ?

A: When an aldehyde or ketone reacts with primary amine then the formation of product is known as…

Q: Show how to convert hexanoic acid to given amine

A: Introduction: To synthesize amine product, firstly hexanoic acid is treated with 1-Methylethylamine.…

Q: Predict the products from the reactions of the following amines with sodium nitrite indilute HCl.(a)…

A: The product from the reactions of the following amines with sodium nitrite in dilute HCl has to be…

Q: 2. Draw the product when each of the amines acts as a base when combined with water, Name the lon…

A: The reactions are as follows:

Q: * The reaction of any carbonyl group with an amine produces the imine true false

A: Dear student since you have asked multiple questions but according to guidelines we will solve 1st…

Q: Indicate whether the following statement is true or false. Aliphatic amines are more basic than…

A: We know that the higher the electron density over nitrogen higher will be the tendency to attract…

Q: A tertiary amine is more basic compared to a secondary amine. (A) True B False

A: Amines are Lewis base due to the presence of a lone pair of electrons on the nitrogen atom of amine.

Q: Write systematic names for these amines

A: The structure of given amine is,

Q: Which amines cannot be prepared by reduction of an amide?

A: Reduction of amides can be done using LiAlH4 to prepare primary (RNH2), secondary (R2NH) and…

Q: Amides undergo hydrolysis under acidic conditions to give Select one: O Carboxylate ion and ammonium…

Q: Be sure to answer all parts. What ammonium salt is formed when this biologically active amine is…

A: Whenever the amine is treated with Acid it get protonated and form Alkyl Ammonium salt .

Q: Draw the structure of the amine salt produced when each of the following amines reacts with HCI. a.…

A: Since you have posted a question with multiple sub-parts, we will solve the first three subparts for…

Q: Which amines cannot be prepared by reduction of an amide?

A: The amines which cannot be prepared by reduction of an amide has to be given,

Q: Draw the product of the SN2 reaction of this amine with one equivalent of methyl iodide. Assume…

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Amide hydrolysis in basic conditions forms A. a carboxylic acid and an amine B. a…

A: Given : Amide hydrolysis in basic conditions forms

Q: Following are structural formulas for two enamines. Me Me క (a) (b) Draw structural formulas for the…

A: Enamine is an organic compound that is formed when an aldehyde or ketone reacts with secondary…

Q: Draw structures for the following amines. - 3-decanamine - N,N-dipropylbutanamine…

A: The IUPAC is a system that contains some rule that helps in the naming of the organic compounds. The…

Question

Define the simplest method to synthesize an amine ?

Definition Definition Organic compounds with a nitrogen atom having a lone pair of electrons on it. Amines are derived from ammonia (NH 3 ), wherein hydrogen atoms are substituted by an aryl or alkyl group.

Expert Solution

Step 1

Amines

Amines are derivatives of ammonia, in which the Hydrogens are substituted by alkyl or aryl group.

The general form of amine is;

R-NH₂

Step 2

Synthesis of amines

the simplest method to synthesize an amine is from alkyl halide.

It involves alkylation of ammonia to form primary amines.

The reaction is;

Ammonia on reaction with methyl chloride produces, ammonium salt, which on treating with base gives methenamine.

Step by step

Solved in 3 steps with 2 images

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

What steps would be used to synthesize an organic amine?
Which type of amine is phentermine? a) a primary aliphatic amine b) a primary aromatic amine c) a tertiary aliphatic amine d) a tertiary aromatic amine
Show how to convert amines to other functional groups, and devise multistepsyntheses using amines as starting materials and intermediates
The hydrolysis of an amide in acidic conditions forms A. a carboxylate salt and an alcohol B. a carboxylate salt and an amine C. an alcohol and an amine salt (an ammonium ion) D. a carboxylic acid and an amine salt (an ammonium ion)
1. Describe the following reactions of amines, include equations if possible a. Hinsberg reactionb. Diazotisation
Draw the structure of the following amin acid.
From the given structures which is(a) amide that will release a secondary amine upon hydrolysis? (b) product of hydrolysis of MSO (c) a tertiary amide and (d) a diketone
Acetaminophen is an analgesic marketed under the brand name Tylenol, among others. Draw the amine that results from the base hydrolysis of acetaminophen.
Aromatic amines are _________ neutral because of the polarity are unique as they do not behave like any of the other amines acidic, but stronger than the aliphatic amines basic, but weaker than aliphatic amines
What is the Methods used to Synthesis of IMINES.
what carboxylic acid and amine is needed to prepare phenacetin
Which type of amine is (s)-methamphetamine? a) a primary aliphatic amine b) a primary aromatic amine c) a secondary aliphatic amine d) a secondary aromatic amine