In the Synthesis of 3,6-dimethyl heptanone, starting from acetoacetic ester, we need * the following reagent Base, acid, and alkylhalide and heating O Base, acid, and alkylgroup and heating Base, H20, and heating O

In the Synthesis of 3,6-dimethyl heptanone, starting from acetoacetic ester, we need * the following reagent Base, acid, and alkylhalide and heating O Base, acid, and alkylgroup and heating Base, H20, and heating O

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter18: Functional Derivatives Of Carboxylic Acids

Section: Chapter Questions

Problem 18.69P

See similar textbooks

Related questions

Q: Which of the following sets of reagents would not be an acceptable method for the preparation of…

Q: Write the reagents used to synthesise the following compound starting from the benzoic acid CH3 ?…

A: Since you have posted multiple questions, we are entitled to answer the first only.

Q: The reagent NaBH4 acts as an ____ 1. H+ (hydride), 2. H- (hydride), 3. H+ (proton), 4. H- (proton)…

A: There are various types of reducing agent which reduces the species. NaBH4 is sodium borohydride,…

Q: Draw the organic products formed in attached reaction.

A: Applying concept of organic synthesis and deprotectanation of functional groups.

Q: Draw a structural formula of the major alkene formed from a reaction of 2-aminoundecane with the…

A: An organic reaction in which the incoming nucleophile takes the position of a leaving group is…

Q: Name the product of the following reaction: BH3, THE H,O2,N2OH

A: It is hydroboration - oxidation reaction .in which first of all BH3 added then oxidation occur in…

Q: Can 4-methylcyclohexanoic acid be reduced by NABH4?

A: The process for the reduction of carboxylic acids is given below. The reaction does not goes…

Q: QUESTION 1 Which of the following alkynes will form only 1 product in an acid-catalyzed hydration?…

A: 1. 1-hexyne is a terminal alkyne. Hence, it will give single product in acid catalysed hydration.…

Q: In the following reaction with H2 and Pd/C, the functional group(s) of the product(s) is(are): Pd/C…

A: The reagent H2 in Pd/C is a reducing agent. In this, the hydrogenation reaction occurs across the…

Q: OH FeCl, + CH3 b. CH3. OH FeCl, + С. OH HO + FeCl,

A: Here we have to write the product of above reaction of phenol, 2-napthol derivative and catechol…

Q: Considering the molecule D-Galactose below, HO- H HO- a. b. H CHO OH H -H -OH CH₂OH Which galactose…

Q: "pentanUI can be preferred to produce aldehyde by the oxidation of 2-methyl-1- 26) The reagent(s)…

A: The mentioned question discusses some concepts about oxidation of alcohol, formation of ester and…

Q: _and a carboxylic 8. An esterification is a reaction in which an ester is formed from an acid. CH =…

A: Ethanoic or acetic acid is used in making dyes, pigments, and paint and coating additives. It is…

Q: The main product was formed for the following reaction HO (R)-2-bromobutane 25 °C

A: For the given reaction : We need to predict the main product of the reaction above.

Q: Esterification reactions, such as the one below, is a poor synthetic strategy as it leads to poor…

A: Carboxylic acid reacts with alcohol in the presence of an acid catalyst to form an ester, the…

Q: In the systematic identification of an unknown organic compound, the preparation of a derivative is…

Q: 10:30 „. 86%| E AIATS For Two Year Medic. 77 /180 (02:54 hr min Mark for Review When ethyne is…

A: When the ethyne is heated with mercuric sulphate and dilute sulphuric acid at 333 K, vinyl alcohol…

Q: Draw the organic products formed in attached reaction

A: The organic products formed in attached reaction can be drawn as,

Q: Which major product is formed when Br2 and H20 are added to 2-methylpropene to give the bromohydrin?…

A: When Br2 and H2o are added to 2-methylpropene, it gives the bromohydrin.The mechanism of bromohydrin…

Q: Which is the reduction product of ethyl 3-oxobutanoate with NaBH4 in methanol? (select the correct…

Q: 4. Which synthesis, starting from benzene, forms aniline (aminobenzene)? a. 1) HNO₂/H₂SO4 b. 1)…

Q: Draw the product of the reaction shown below. Ignore inorganic byproducts. Но OH H2SO4

A: This is an example of a dehydration reaction. Here, ether formation takes place when proton attacks…

Q: - 90 gm of acetic acid can be obtained by oxida [C=12, 0=16, H=1] (a) 69 gm of ethanol (b) 44 gm of…

A: Ethanol under oxidative condition produces acetic acid.

Q: Preparation of carboxylic acid V. From Acyl Halides and Anhydrides Type of Reaction: chemical…

A: • By the hydrolysis of acid derivatives acid can formed. • Acyl halide reacts with alkoxide in…

Q: Name the product obtained in the following reaction, the catalyzed hydrogenation of 2-butanone.…

A: 2-butanone undergoes catalytic hydrogenation to produce 2-butanol.

Q: Which type of reaction would convert 1-hexanol in hex-1-ene? A) Hydration Acid-Catalyzed Dehydration…

Q: Name the reaction H2SO4 R R R. H20 1) R2BH R =H R. H. 2) NaOH, H2O2 O Hydration O…

A: Answer given as follows

Q: Draw a structural formula of the major alkene formed from a reaction of 2-aminoundecane with the…

A: The given reagent used for elimination reaction.half mann product is major.

Q: After performing all of the necessary calculations, the appropriate glassware and reaction…

A: The hydrolysis reaction taking place is given as,

Q: (a) pyridine + CH3COOH acetic acid N H pyrrole + CH3COOH acetic acid

Q: 3. The reaction of a group once when it might react twice as in thiol synthesis. Na₂S R Br R R R Br…

A: Hello dear, Compound 8 is more reactive.

Q: Produced by the reaction of formaldehyde with e 2-thiothiophene : secondary alcohol carboxylic acid…

Q: Write the products of the following reactions: (all reactions are a nitration) 2. H* HNO3 (MECO),0

Q: What is the reactant and product of reduction of 2,4-dimethyloctanoic acid by 1. LiAlH4 reaction…

A: LiAlH4 reduces carboxylic acid so as to form corresponding alcohol.

Q: what is the product of a reaction between C10H16(terpinene) +maleic anhydride

Q: 2. In the hydrolysis of amide, what is the identity of the leaving group? Whai are the final product…

A: Hydrolysis of amide means the reaction of amide with water but the reaction is slow so acid catalyst…

Q: In an esterification reaction, a carboxylic acid reacts with an excess of alcohol in acidic…

A: Given :- pentanoic acid+ 1-propanol→ ester+ H20 To draw :- Structure of ester formed in this…

Q: Consider the following reaction: H. NaOH `PPH3CI Ph3P=O в A: 9-anthraldehyde Calculate the…

Q: The main product was formed for the following reaction * HO (R)-2-bromobutane 25 °C

A: We are to predict the product formed when (R)-2-bromobutane reacts with OH– at 25°C

Q: In Experiment 66: An Oxidation Puzzle, one alcohol on the starting material was selectively oxidized…

Q: The reduction of 4- nitrobenzaldehyde using sodium borohydride,MaBH4 in ethanolwhich is not a…

A: Reduction is a type of chemical reaction in which the oxidation states of atoms are changed.…

Q: responsible for this hibernation. HO HO OH Daumone Ester O Alkyne Ерохide O Arene Carboxylic Acid O…

Q: Draw the products formed in attached reaction.

A: The Heck reaction is the reaction of an unsaturated halide and an alkene in the presence of a base…

Q: The product for the following reaction is a/an: 1. TsCl, Pyridine HO 2. Sodium Acetate O a.…

A: TsCl convert alcohol into good leaving group.

Q: Which Grignards would be required to complete the following reactions? Use condensed formula for…

A: The reactions taking place are,

Q: Hydration of aldehydes and ketones can be catalyzed by acid or base. Acids catalyze hydration by:…

A: To choose: The correct option for acid catalyzed hydration of aldehyde and ketone by acid.

Q: What carboxylic acid is used to prepare this ester?

A: The ester prepared is given as,

Q: Draw the structure of the major organic product(s) of the reaction. CH30. H20 CH3Ó • You do not have…

Q: Draw the structures of the neutral organic products formed in the following reaction. Do not draw…

A: Please find below the mechanism for the reaction taking place.

Question

In the Synthesis of 3,6-dimethyl heptanone,
starting from acetoacetic ester, we need
* the following reagent
Base, acid, and alkylhalide and heating O
Base, acid, and alkylgroup and heating O
Base, H20, and heating

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 3 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

22. Provide the following: 1) the major organic product of each reaction shown, and ii) the specific name of the reaction in the first step. aniline AICI (if o,p-substituted products are possible, only provide the major para-substituted product, otherwise, only provide the meta-substituted product) 12, HNO (if o,p-substituted products are possible, only provide the major para-substituted product, otherwise, only provide the meta-substituted product) end a chat
a) A specific example of the Curtius rearrangement of an acyl azide to an isocyanate. b) The anionic intermediate that undergoes rearrangement in the Hofmann rearrangement below. 2 equiv NaOH, „NH2 NH, Br, H20 CO2 c) The iminium ion that is reduced in the in the reductive amination below. d) The Michael addition adduct that is generated in the Robinson annulation below. catalytic NaOCH3, CH;OH H3C + H20 рH 45 A NABH;CN CH;ÓH
1// In a set of the given reactions, acetic acid yielded a product C C6 H6 C HM9B CH;COOH + PCl, → A anh. AlCl ether What would be product C? 2// When propionic acid is treated with aqueous sodium bicarbonate formed? 3// When CH3COOH reacts with CH3-Mg-X formed? 4// What is the product in the given reaction when benzyl chloride reacts with benzen?
The final products for the hydroxide-ion-promoted hydrolysis of an ester re the carboxylate ion and methanol instead of the carboxylic acid and methoxide ion. Why?
Give the major product of the following reaction. NaOH H* ? -CI heat
9) a) Diagram the acid (H3O+) catalyzed enolizaton of acetaldehyde. . b) Diagram the base (OH-) catalyzed formation of cyclopentanone from its enol form.
Synthesize 2-methylbutanoic acid from 2-methylbutene. Please provide all steps and reagents used.
A Give the main organic product that would form after the following reaction. OMe OMe H₂O H* I
3-Hexanone can be synthesized from butanal and ethane using a Grignard reaction. The first step must be O creation of a carbocation O protonation of an oxygen nucleophilic attack of the aldehyde free radical halogenation preparation of an acetylide
b) The Wolf-Kishner reduction is a reaction used in Organic Chemistry to convert carbonyl functionalities into methylene group. The reaction was used to convert an aldehyde or ketone to an alkane using hydrazine, base and thermal conditions. The mechanism begins with the attack of hydrazine of the aldehyde or ketone. Stage 1: The reaction of aldehyde/ketone with hydrazine to produce hydrazine Stage 2: Reaction with the base and heat to convert hydrozone to alkane Write the mechanism of the reaction.
In biochemical reactions, decarboxylation of carboxylic acids typically takes place for-keto carboxylic acids. Justify a rational why nature opted for-keto carboxylic acid decarboxylation. Among the following types of biochemical reactions, ester hydrolysis, rearrangement reactions, water elimination reactions, and anhydride hydrolyses, which one is the most favorable one. Rank the above reactions types in the order of being the most to least favorable reaction
Define the following reagents or functional groups as being related to either aldehydes/ketone AK, carboxylic acid derivatives CA or both. Imines Acid anhydrides Hemiacetal Aldol i) LIAIH4 ii) H+, H20 Haloform