Answered: 57. What will be the product if…

57. What will be the product if aldehyde reacts with NaOH? Benzyl alcohol Benzoic alcohol а. b. Hydrobenzamide Cinnamic acid с. d.

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

Chapter14: Aldehydes And Ketones

Section: Chapter Questions

Problem 14.36E: Not all aldehyde give a positve Bendicts test. Which of the follwing aldehydes do? a. d. b. e. c.

See similar textbooks

Related questions

Q: What reagents would you use to convert methyl propanoate to the following compounds? a. isopropyl…

Q: Draw a stepwise mechanism for the sulfonation of an alkyl benzene such as A to form a substituted…

Q: Why is it not advisable to use aqueous hydrochloric acid in a Grignard reaction of a ketone? A) The…

A: Alkyl magnesium halide is known as a Grignard reagent. The general formula of the Grignard reagent…

Q: Order the compound according to increasing boiling point: a) 3-pentanone b)2-methylcyclopentene…

A: Boiling point depends on the intermolecular forces acting between the molecules. The more are these…

Q: When bromoethane is refluxed with KOH in an alcoholic medium, compound Y is formed. Give the…

A: Alkyl halides on heating with alcoholic KOH undergoes dehydrohalogenation and an alkene will be…

Q: Draw structural formulas for the a,ß-unsaturated aldehyde or ketone and the lithium diorganocuprate…

A: please find attached the required answer

Q: 2. What carboxylic acid and alcohol are needed to prepare each ester by Fischer esterification? a)…

Q: In an experiment, triphenylmethanol is prepared using the Grignard reaction. The Grignard reaction…

A: The Grignard reagent is a strong nucleophile that magnesium attached to a halogen group and an alkyl…

Q: What carbonyl compound and Grignard reagent could be used to prepare 2-butanol?

A: The species possessing general formula RMgX are helpful in carbonyl compounds to alcohol conversion.…

Q: Which ketone cannot be made by the acid catalyzed hydration of an alkyne? A B C D E

Q: Draw a stepwise mechanism for the following reaction of a Grignard reagent with a cyclic amide.

A: Given,

Q: Would thioesters be expected to be more or less reactive to hydrolysis than esters? Explain.

A: The question is based on the concept of organic reactions. we have to account for different…

Q: Write reactions of 3-methylbutanal with the following reagents: c. CH3OH/H+; d. CH3NH2;

A: We will write the product

Q: Write reactions of aniline with the following reagents: a. CH3COCl b. Br2 c. CH3I

A: (a) The reaction in which aniline reacts with acid chlorides, the final product of the reaction will…

Q: a. How can aspirin be synthesized from benzene?b. Ibuprofen is the active ingredient in pain…

A: Given:

Q: (b) Draw the chemical structure of a 1,2,3-triazole and showv how it can be synthesized from basic…

A: 1,2,3 Triazole is an aromatic heterocycle which has numerous applications

Q: which among the organic liquids best match compound b based on its reaction to the various reagents?…

A: For the determination of organic compounds, it is reacted with some reagent to see what visual…

Q: Why do water-insoluble carboxylic acids dissolve in aqueous sodium hydroxide? 38.

A: To explain why water-insoluble carboxylic acids dissolve in aqueous sodium hydroxide.

Q: What

A: First OH- attack on carbonyl carbon and then π bond transfer towards more electronegative atom…

Q: Thiols or thiol (-SH) group is a better base than hydroxide (-OH) group in elimination reactions.

Q: Draw a stepwise mechanism for the formation of A from an alcohol and acid chloride. A was converted…

A: Since the alcohol group is having lone pair electrons and hence can attack on electrophile And…

Q: 10. Write chemical equations for the reaction of ethyl propanoate with each reagent below. a)…

A: Given: Ethyl propanoate To find: the products with each of the reagent LiAlH4/H3O+ NH3 C2H5NH2 NaOH

Q: Acetanilide is less reactive than aniline toward eletrophilic substitution. Explain.

Q: (a) How will you convert:(i) Benzene to acetophenone (ii) Propanone to…

A: Benzene can be converted into acetophenone by reacting benzene with acetyl chloride in the presence…

Q: The reaction of a ketone and excess methanol with an acid as a catalyst gives what product? A)…

A: When alcohol is added ketone in presence of acid hemiketal is formed.When excess alcohol is added…

Q: t. acetic acid + PCl; u. pent-3-en-2-one + methanol v. butanone + 2 equivalents of methylamine and…

Q: 26. What type of bond promotes the solubility of alcohols in water? A. Hydrogen bonds B.…

A: 26. Option (a) Alcohols are soluble in water. This is due to the hydroxyl group in the…

Q: 46. Which carbonyl group of the given compound is most reactive for nucleophilic addition reaction?…

A: The answer of all questions have been outlined below

Q: The diol shown undergoes reactions with reducing and oxidizing agents to yield two different…

A: Given : We have to draw the product for the given reactants.

Q: Consider the two-step synthesis of 2-hydroxy-2,4-dimethylpentanoic acid using the reagents provided.…

A: The prussic acid is another name of hydrogen cyanide having formula HCN. This hydrogen cyanide is a…

Q: What structural and/or molecular properties of aldehyde/ketonecontributes to their reactivity with…

A: Ag2O+4NH3+H2O→2Ag(NH3)+2+ 2OH− (Tollens reagent)

Q: What product is obtained when the following vicinal diol is heated in an acidic solution?

A: Please find below the reaction

Q: Give the products formed when benzaldehyde and benzoic acid are treated with the given reagents. a.…

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: 16. If toluene is synthesized from benzene and methyl chloride, what reaction has been observed? A.…

Q: Although 2-methyl-1,2-propanediol is an unsymmetrical vicinal diol, only one product is obtained…

A: vicinal diol is a compound with two -OH groups on adjacent carbons.…

Q: [ 12] what is major product of following ? SOCI2 phenol HO, ? ( a) benzylacetate (b) phenylacetate…

A: The answer is given as follows

Q: Describe the reaction when a. Formaldehyde mixed with a fainty pink solution of potassium…

Q: Why is it unwise to begin addition of the solution of carbonyl compound to the Grignard reagent…

A: Grignard reagent is a base and the reactant being a good acid and the reaction between will result…

Q: 38. What type of reaction is observed below? you-l-fynd A. Acylation B. Alkylation C. Markovnikov D.…

Q: 2-Pentanol when introduced with H2SO4 will become ____________ . H2SO4 is a Dehydrating agent…

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

Q: Consider carbonyl compounds A– E attached below. Which compound is most reactive in nucleophilic…

A: The stability of the carbonyl compound can be determined by the electrophilic character of the…

Q: 2. How many different ß-hydroxyaldehydes and ß-hydroxyketones, including constitutional isomers and…

Q: Explain WHY/HOW all please - Propanol CANNOT protonate ethylamine - 3-methylheptan-3-ol CANNOT be…

A: Since you have asked a question with multiple subparts, we will answer only first three subparts for…

Q: Convert benzene into attached compound. You may also use any inorganic reagents and organic alcohols…

A: The formation of grignard reagent is shown below.

Q: The reaction of a nitrile with an alcohol in the presence of a strong acid forms an N-substituted…

Q: According to the pharmacopoeia, the diphenylamine reaction is an authenticity reaction to? A)…

A: Sodium nitrite (NaNO2) is an oxidising agents oxidise diphenylamine giving deep blue colour.

Q: MCQ 18: The solution which is used to detect the presence of aldehyde or ketone is A.…

A: Tollen's Reagent: It can be prepared by the following given methods: 1 Addition of silver nitrate…

Q: Explain the solubility behavior of each compound in water with relevance to their structure. a.…

Question

please explain thanks!

57.
What will be the product if aldehyde reacts with
NaOH?
Benzyl alcohol
Benzoic alcohol
а.
b.
Hydrobenzamide
Cinnamic acid
с.
d.

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 steps with 1 images

SEE SOLUTION Check out a sample Q&A here

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

Not all aldehyde give a positve Bendicts test. Which of the follwing aldehydes do? a. d. b. e. c.
Complete the reaction: 42K19 → + β + [a]_____________
4. WHAT ARE IMINES? HOW ARE THEY FORMED? 5. WHAT IS GRIGNARD REACTION? WHAT CONSTITUTES A GRIGNARD REAGENT? 6. WHAT IS KETO-ENOL TAUTOMERIZATION?
When ethyl acetate and sodium bicarbonate were mixed together, clumping of solid was observed. Did ethyl acetate react with sodium bicarbonate (NaHCO3)? Why or why not?
2. Draw the reaction scheme in ChemDraw depicting Strecker aldehyde starting from α-dicarbonyl. Include general reactants and by-products as necessary.
The reaction of a nitrile with an alcohol in the presence of a strong acid forms an N-substituted amide. This reaction, known as the Ritter reaction, doesnot work with primary alcohols. a. Why does the Ritter reaction not work with primary alcohols? b. Provide an explanation for why an amide is less susceptible to nucleophilic attack than its corresponding ester.
Define Reaction of Acetylide Anions ?
57. What are the nucleophile and electrophile in the cyclization of glucose below?
Describe the preparation (E and F only)
Classify the reaction type. a. oxidation (Benedict's) b. reduction (hydrogenation) c. acetal formation d. hemiacetal hydrolysis e. acetal hydrolysis f. mutarotation g. hemiacetal formation
a) Put these three common types of carbonyl compound in order of decreasing reactivity ester amide acid chloride b) For the least reactive, show the interconversion to its other resonance form: How does this electron delocalisation make it stable? c) For the most reactive, draw the mechanism of its undergoing hydrolysis (reaction with H2O): Why makes this type of carbonyl so reactive to nucleophiles?