heat CH3- -Ĉ-OH+NH3

Q: Draw the products formed when each amine is treated with [1] CH3I (excess); [2] Ag2O; [3] Δ.…

A: Solution: a) part Product formed is given below when treated with [1] CH3I (excess); [2] Ag2O; [3]…

Q: Complete the electron-pushing mechanism for the following base-promoted hydrolysis of an amide. Add…

A: Substitution reaction involves the replacement of a functional group with an another. Nucleophile is…

Q: Amines can be prepared by converting other functional groups. Classify these reactions and choose…

A: The conversion of nitrile to amine is a reduction reaction. The conversion of Nitro group to amine…

Q: Use this amine to answer the following questions: A) Is this amine primary, secondary or tertiary?…

A: (a) Is this amine primary, secondary or tertiary? (b) Draw the product when this amine reacts with…

Q: 2. Which member of each of the following pairs of molecules has the higher boiling point? a.…

A: A substance's boiling point is the temperature at which the vapor pressure of a liquid equals the…

Q: likely to form when reacting Ethyl amine and excess ethyl

A: Organic reactions are those in which organic reactant react to form organic products. We have to…

Q: Click on the compound that would give the amide (shown below) the best yicld when treated with…

A: The more reactive acid derivative can be converted into less reactive acid derivative by the…

Q: Draw the structure(s) of the major product(s) of the following reaction after workup to neutralize…

A: (S)-Coniine on treatment with benzyl chloride forms a product and was worked up with base to…

Q: HNO3 H₂SO4 F X Predict the major product for each of the for H₂ Pt NaN, H₂ Pt H 1) Fe, Zn, Sn, or…

A: nitro group and azide groups are reduced in presence of reducing agent that leads to producing amine…

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

A:

Q: Which of the following statements is correct? O a. All esters are weak bases O b. All ethers are…

A: a. Esters: esters have two lone pairs on  O atom but being highly electronegative oxygen can't…

Q: Select the name for each amide. ye ON-ethylpropanamide N-methylbutanamide N-butylethanamide…

A: In the IUPAC nomenclature first we have to find the functional group containing long chain. The…

Q: Activity 1: 1. Classify each of the following amines as primary, secondary or tertiary. CH,CH,…

A:

Q: what happens when an amide reacts with water?

A:

Q: draw the following

A: Name to structure: In general name of a compound is in the order of prefix + rootword + suffixRoot…

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

A:

Q: Select the amide formed by this reaction (water is also formed). Assume that a reaction occurs, even…

A: Reaction of amines and carboxylic acids in the presence of thionyl chloride leads to the formation…

Q: Please use Henry reaction to find the "A" product, a trans alkene product. The "A" product can…

A: In this question, we want to identify Product A and B  How we can identify, I will give details…

Q: Oxytocin, sold under the trade name Pitocin, is a naturally occurring hormone used to stimulate…

A: The amide functional group i.e O=C-N is classified as  1°, 2°, or 3° based on the number of carbon…

Q: Draw the mechanism of the acid catalyzed hydrolysis of the two following compounds. The products…

A: In the given question we have to do the acid catalysed hydrolysis of ester and amide functional…

Q: Draw the major product of this reaction. Ignore inorganic byproducts and the amine side product.

A: The major organic product of the reaction is cyclohexanecarboxylic acid.Explanation:

Q: How is the nitrogen of the oxazole similar or different to the two nitrogen’s that are found in the…

A:

Q: Which of these would likely take the LONGEST to hydrolyze (undergo hydrolysis) to the carboxylic…

A: The reactivity of carboxylic acid derivatives is as follows  Acid chlorides > Acid anhydrides…

Q: 5) Circle the strongest base. 4-chloroaniline 4-nitroaniline 4-aminobenzonitrile ABCDE C. D. aniline…

A:

Q: 9. Amides are less basic than amines because: a. the carbonyl group donates electrons to the amide…

A:

Q: Choose the right answer

A: Basicity of amine directly proportional to the avalability of lone pair electron on nitrogen atom.…

Q: I. Give the reaction on how to convert the following amides. Include the IUPAC name and draw the…

A: (A) Compound A can be prepared by Reaction between dimethyl amine and heptanoic acid, as -

Q: Arrange the compounds  in order of decreasing basicity A. ethylamine B. 2-aminoethanol C.…

A: The given compounds are, Ethylamine 2-aminoethanol 3-amino-1-propanol

Q: NH NH2 NH2 WXY ZAB CDE FGH IJK least basic amine Choose... + most basic amine Choose... + most…

A:

Q: N. NH2 a b N N. d I Z

A: The basicity of Amine depend upon various factors such as . Delocalization of lone pair effect.…

Q: Reactions of aldehydes and ketones with amines and amine derivatives a. Draw reaction with a primary…

A: Amines is considered as organic derivatives of ammonia where alkyl groups replace the hydrogen atoms…

Q: Draw the product that will form if the amine in Figure 25 reacts with hydrochloric acid in an…

A:

Q: Please answer question no. 10

A: 10. Given statements: a. Esters are more reactive than acid anhydrides. b. Amides are easily…

Q: g) h) Br Br type type i) Ph. N. type Ph NaOEt/EtOH a) NaBH4/CH3OH b) H3O+ H3O+ imine hydrolysis +

A: The question is based on organic reactions.We need to identify the product and explain its…

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: 3. If the compound shown is subjected to reaction conditions that will hydrolyze amides one of two…

A: Solution of the question is given below:

Q: F Draw the major product of this reaction. Ignore inorganic byproducts and the amine side product.…

A: Given,The reaction is:

Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.