Which of the alkyl chlorides listed below undergoes dehydrohalogenation in the presence of a strong base to give 2-pentene asthe only alkene product?Select one:A. 1-chloropentaneB. 3-chloropentaneC. 2-chloropentaneD. 1-chloro-2-methylbutaneWhich of the following is the most stable species?Select one:CH3A.о в.H3C CH3O D.

Since your question has multiple parts, we will answer the first question for you. If you want…

hich of the alkyl chlorides listed below undergoes dehydrohalogenation in the presence of a strong base to ne only alkene product? Celect one: O A. 1-chloropentane B. 3-chloropentane C. 2-chloropentane D 1-chloro-2- mothylbutane

hich of the alkyl chlorides listed below undergoes dehydrohalogenation in the presence of a strong base to ne only alkene product? Celect one: O A. 1-chloropentane B. 3-chloropentane C. 2-chloropentane D 1-chloro-2- mothylbutane

Pushing Electrons

4th Edition

ISBN:9781133951889

Author:Weeks, Daniel P.

Publisher:Weeks, Daniel P.

Chapter3: Mechanisms

Section: Chapter Questions

Problem 110EQ

See similar textbooks

Related questions

Q: Draw a stepwise mechanism for the conversion of dihalide A and cyclohexane-1,4-diol to polyether B…

A: Since AlCl3 is a Lewis acid and hence it will extract Cl from the compound A forming a carbocation…

Q: a 그 b. ~

A: To find: reagents used to prepare the next alkene.

Q: Dehydration of 1,2,2-trimethylcyclohexanol with H2SO4 affords 1-tertbutylcyclopentene as a minor…

A: a.

Q: A. Oxidation of 2° alcohol to a ketone Reagents: Jones Reagent (CrO3 in aquous H₂SO4; acetone)

Q: Draw the major product of this reaction. Ignore inorganic byproducts. 1. CH3LI 2. H3O*

A: Major product of the given reaction = ?

Q: Consider the conversion of alkyl halide A to ether B. a.Classify the conversion of A to B as…

Q: CI FeCl3

A: To complete the above reaction,

Q: Select the reagent you would use to form Product B. H2SO4, H2O OLDA OTS O NaCN O H2O elimination 20"…

Q: major product formeEU in the ving reaction is: Br NaOMe COOME (a) (b) (d)

A: In this reaction NaOme reacts with Br so carbocation will form and as carbocation form double bond…

Q: N-Chlorosuccinimide (NCS) serves as a source of Cl+ in electrophilic addition reactions to alkenes…

Q: What alkene can be used to prepare each alcohol as the exclusive product of a two-step…

A: The reaction in which boron and hydrogen is attached to the alkene and formed alcohol is known as…

Q: Draw all possible constitutional isomers formed by dehydrohalogenation of each alkyl halide.

A: a.

Q: Draw the most stable form of the major mixed Claisen product formed in the following reaction. 1.…

A: Step 1: Extraction of acidic hydrogen from ethyl acetate takes place not from ethyl isobutyrate due…

Q: What products are formed from reaction of one mole HCI with this ether ? (Hint: CI is a weak…

A: The ether is the organic compound formed by the combination of two alcohol molecules. The…

Q: Compare These TWO reaction a and G Which both produces alkene Expluin what are the major differenLes…

Q: N-Chlorosuccinimide (NCS) serves as a source of Cl+ in electrophilic addition reactions to alkenes…

A: Since alkyne is a nucleophile. hence the Cl+ produced by the N-Chlorosuccinimide will be attacked by…

Q: What alkene is the major product formed from attached alkyl halide in an E1reaction?

A: E1 reactions are two step reactions in which the first step is the cleavage of carbon halogen bond…

Q: Draw a stepwise mechanism for the conversion of dihalide A and cyclohexane-1,4-diol to polyether B…

Q: Consider the conversion of alkyl halide A to ether B. Question: Classify the conversion of A to B as…

A: A reaction in which one group or atom is replaced by other atom or group is known as substitution…

Q: Please the follawa Componds Synthesize tram benzene Notc A Friedel -Crafts alky la tro wont wer…

A: The synthesis of 4-chloro toluene involves two reaction, first Friedel-Crafts alkylation and then…

Q: 1. Show the organic product formed when pentanal is heated with sodium methoxide in methanol as…

Q: prrect? :0: :0? CH3- CH2-C-CI: CH3- CH2-C- H H-ö: H A. The alcohol is a nucleophile in this

A: Nucleophile is the electron excess species. So, Alcohol is act as Nucleophile. Positive charge on…

Q: Dehydration of 1,2,2-trimethylcyclohexanol with H2SO4 affords 1-tert-butylcyclopentene as a minor…

A: a) The stepwise mechanism that describes the formation of 1-tert-butylcyclopentene is as follows,…

Q: Draw the structure of a dihalide that could be used to prepare each alkyne. There may be more than…

A: a. Required alkyl dihalide for the preparation of compound 2-butyne is 2, 2-dibromo-butane or 2,3…

Q: 39) Why is there a need for a higher temperature set-up in elimination reactions? a. Because…

A: Elimination reactions are those reactions in which single bond is converted into multiple bond. For…

Q: Lx Grve Up? In each reaction box, place the best reagent and conditions from the list. 1) 2) 3) 4)…

A: In this question, we determine all best Reagent for this transformation. I will give complete…

Q: Label the a and B carbons in each alkyl halide. Draw all possible elimination products formed when…

A: Biomolecular elimination (E2) reaction: E2 reaction involves a one-step mechanism in which…

Q: Synthesize each compound from acetylene. You may use any other organic or inorganic reagents.

A: Reagent:- It is the reactive substance which attacks at less reactive reactant (called as substrate)…

Q: Draw compounds B and C from the following reaction scheme. excess CH3I Ag20, H20 heat A B

A: In presence of excess of CH3I followed by oxidation by silver oxide, amines undergo Hoffmann…

Q: Draw a stepwise mechanism for the conversion of dihalide A andcyclohexane-1,4-diol to polyether B in…

A: The stepwise mechanism is given below -

Q: Label the α and β carbons in attached alkyl halide. Draw all possible elimination products formed…

A: Biomolecular elimination (E2) reaction: E2 reaction involves a one-step mechanism in which…

Q: An acid catalyst in nucleophilic addition of aldehydes and ketones is used for: Select one: O a.…

A: 1.) We would use a reaction to predict the use of acid catalyst in the reaction. 2.) Difference in…

Q: Why some substituents make a benzene ring react faster than benzeneitself (activators) ?

A: Directive influence of the attached substituents on the benzene ring The ability of the attached…

Q: Draw a stepwise mechanism for the conversion of lactone A to ester Busing HCl in ethanol. B is…

Q: B most, A least O A most, B least O A most, Cleast Question 18 H3C H. CH3 H;C CH3 Which would be the…

A: This reaction involves conversion of alkyne to trans alkene.

Q: Dehydration of 1,2,2-trimethylcyclohexanol with H2SO4 affords 1-tert-butylcyclopentene as a minor…

A: (a) part Treatment of 1,2,2-trimethylcyclohexanol with H2SO4 gives 1-tert-butylcyclopentane. Thus,…

Q: Ethers are oxidized with O2 to form hydroperoxides that decompose violently when heated. Draw a…

A: The above reaction takes place via a free radical mechanism.

Q: What alkene or alkyne yields each set of products after oxidative cleavage with ozone?

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

Q: Which halide is most reactive in SNl reactions? Select one: CI CI H3C CI CH3 CH2CI CI

A: The SN1 reaction is a nucleophilic substitution reaction. It is a two-step reaction where the first…

Q: b) CH3-CH-CH-CH; ОН ОН frpm CH3-CHOH-CH,-CH3

Q: Consider the energy diagram shown below when answer questions A- В C D FG E Progress of Reaction (a)…

A: The given energy diagram is shown below :

Q: QII: Starting from toluene as the only organic reagent you have and use any other inorganic reagents…

A: The preparation of the given compound can be done from toluene by using Friedel craft alkylation…

Q: 3 Organic Chemistry, helppp with ALL PARTS(A&B) Consider the monoterpene linalool, a natural product…

A: When alcohol treated with strong protic acid, such as sulfuric or phosphoric acid then dehydration…

Q: B. Draw the structure of the alkyl bromide and alcohol that must be used to prepare the following…

A: Alkyl bromide reacts with alcohol to form an ether by the Williamson ether synthesis. The reaction…

Q: QVI: Starting from benzene as the only organic reagent you have and use any other inorganic reagents…

A: Starting from benzene, nitration would yield nitrobenzene and further reaction with xenon fluoride…

Q: Draw a stepwise mechanism for the conversion of dihalide A and cyclohexane-1,4-diol to polyether B…

A: First the Lewis acid, AlCl3 takes chlorine from dihalide compound A results to form AlCl4- and…

Q: LIOH, H2O ??? heat

A: Given incomplete reaction is : What is the starting material = ?

Concept explainers

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.

Question

Which of the alkyl chlorides listed below undergoes dehydrohalogenation in the presence of a strong base to give 2-pentene as
the only alkene product?
Select one:
A. 1-chloropentane
B. 3-chloropentane
C. 2-chloropentane
D. 1-chloro-2-methylbutane
Which of the following is the most stable species?
Select one:
CH3
A.
о в.
H3C CH3
O 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

In the reaction below, 3-Buten-2-one reacts with 2,3-Dimethyl-1,3-butadieneand 1,3-Butadieneat 140°C and 30°C, respectively. Explain why these two dienes react at different temperatures.
1. Write in the product of 1-Fluoro-3,7-dimethyl oct-4-yne with these reagents a) ---excess H2,Pd/C----> b) ---Na, NH3------------> c) ---H2, Lindlar catalyst-->
What would the final products look like? Pls specify stereochemistry if needed
Please name the alkenes that yield 3-methylheptane on the catalytic hydrogenation Thank you
A chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under thesame conditions, the reaction of (2S,3S)-3-bromo-2,3-diphenylpentane gives two alkenes, A (cis-trans mixture) and C.Upon catalytic hydrogenation, all three of these alkenes (A, B, and C) give 2,3-diphenylpentane. Determine the structuresof A, B, and C; give equations for their formation; and explain the stereospecificity of these reactions
In an attempt to prepare propylbenzene, a chemist alkylated benzene with 1-chloropropane and aluminum chloride. However, two isomeric hydrocarbons were obtained in the proportion of 2: 1. What is the main product? How did this come about? Explain showing the mechanism and nomenclature of the reaction compounds
Which alkene from the choices can react with excess Hbr to yield the major product shown in the first photo?
Introduce the reaction and structure of the expected products (indicate the main product, when possible) for a reaction of 3-ethyl-5-methyl-hex-2-ene with the following reagents: (a) Br2, CH2Cl2 (b) H2O , Diluted H2SO4.
Hydration of alkynes (via oxymercuration) gives good yields of single compounds only with symmetrical or terminalalkynes. Show what the products would be from hydration of each compound.cyclodecyne
CH₂ + Using the reagents below, list in order (by letter, no period) those necessary to prepare 2-butyne from acetylene. Note: Not all spaces provided may be needed. Type "na" in any space where you have no reagent. a. Br₂, heat, light b. Na, (-H₂) c. Nal(SN2) d. NH4NO3 e. 1) NaNH2, liq. NH3, 2) CH3Br f. (CH3)3COK, (CH3)3COH, heat g. NaOEt, EtOH, heat Step #1 Step #2 Step #3
An inexperienced student adds a solution of catalytic H2SO4 and water to the alkene shown below, expecting to produce 1-cyclobutylethan-1-ol.
20- Show and write the correct reactions of the addition of 2 moles of HBr to 1-Hexyne.21- Tautomerization is a process in which an enol yields a ketone Give one examplefor a keto to enol tautomerization. Which form is more stable. Also, which ismore stable the E isomer or the Z isomer of 2-Chloro, 2-Butene?