The compound below undergo elimination reaction to produce 2 types of alkenes. Based on Zaitsev rule, what will be the major product of this elimination? ОН O a. 2-methylpent-4-ene O b. 4-methylpentene c. 4-methylpent-2-ene

The compound below undergo elimination reaction to produce 2 types of alkenes. Based on Zaitsev rule, what will be the major product of this elimination? ОН O a. 2-methylpent-4-ene O b. 4-methylpentene c. 4-methylpent-2-ene

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 26CTQ

See similar textbooks

Related questions

Q: What alkenes are formed from attached alkyl halide by an E2 reaction? Use the Zaitsev rule to…

Q: 1) Complete the chemical reaction and write the type reaction whether SN1 or SN2 or E1 or E2 or…

A: H2O favours substitution reaction . Strong base favours elimination reaction.

Q: The Stille reaction is similar to the Suzuki reaction. It replaces the alkenyl-organoboron compound…

A: Stille reaction is an organic chemical reaction in which organic compounds are synthesized with an…

Q: Q4 Which statement below about Sn1 reactions is incorrect? (A) SN1 reactions are stepwise and have…

A: A chemical reaction mechanism represents the way to form and break the chemical bonds between…

Q: 1. KMNO4, HO, Hа0, heat CH3 2. HС H,C- Product 2 ČH3

Q: a) Br (only product) b) I I ( CH₂CHCH₂CHCH₂ C) H₂₂C A Br H₂C CH₂

A: Preparation of molecules given using any alkene:

Q: How many elimination products would be formed using the molecule below as the starting material?

Q: What alkenes are formed from each alkyl halide by an E1 reaction? Use the Zaitsev rule to predict…

A: E1 reactions: These reactions proceed in two parts. Lose of leaving group. Removal of proton These…

Q: Which alkyl bromide(s) can form the alkene under E2 elimination conditions

Q: Q4 Which statement below about Sn1 reactions is incorrect? (A) SN1 reactions are stepwise and have…

A: Given statements, (A) SN1 reactions are stepwise and have intermediates. (B) The slow step in a SN1…

Q: Which method is suitable for converting 2-hexyne to (Z)-2-hexene? A. Na or Li in liquid NH3 B. H2,…

A: Alkynes are the organic compounds which contains at least one triple bond present in it. While…

Q: 8. ******* Which involve large number of organic reaction donot involve and free radicals OA.…

A: Organic reactions are proceeded by many mechanisms like addition, substitution, elimination, etc.…

Q: The two reactants shown below are combined to bring about a nucleophilic substitution reaction.…

Q: A benzene ring reacts with these reagents in order: 1) Cl2, AlCl3 2) Mg 3) CH3CH2CHO 4) H + 5) conc.…

A: Following reaction occur with the benzene in the order as-

Q: Show the steps necessary, in order, to make each of the following compounds. Start with benzene, and…

Q: When 3-bromo-2,3-dimethylbutane is heated in sodium tert-butoxide, one major alkene is formed. In…

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Which of the following carbocations would rearrange after reaction with HX? a. Хон b. ҳ CA ОН 'OH

A: -> When alcohol reacts with hydrogen halide Reaction proceeds through formation of carbocation…

Q: 4. Draw the structure for the product formed in each of step of the following synthetic sequence.…

A: Given, The products formed in each step of the synthesis is:

Q: Rank these alkyl halides in order of increasing reactivity in an SN2 reaction. A) III < I < || II…

Q: How many alkene products, including E, Z isomers, might be obtained by dehydration of…

Q: 10. Classify the following alkenes as E or Z: CH3 Cilz0H • CH2 Br Citz0 NHz

A: The absolute configuration of alkenes are substituent dependent. The arrangement of substituents of…

Q: Draw Out Your Predictions of This Reaction: Part A: S-2-chlorohexane + NaOCH3NaOCH3 in methanol.…

Q: In both examples below the reactants shown are combined to bring about a nucleophilic substitution…

Q: Match the species with the description of its reactivity. alkene chloride 1. nucleophile carbocation…

Q: А. В. С. D.

Q: What alkenes are formed from attached alkyl halide by an E2 reaction? Use the Zaitsev rule to…

A: E2 elimination is a bimolecular elimination reaction. It is a 2nd order reaction involving the…

Q: What alkenes are formed from each alkyl halide by an E2 reaction? Use the Zaitsev rule to predict…

A: Given compounds,

Q: Part A Which alkene should be used to synthesize the following alkyl bromide? Interactive 3D display…

Q: 1-butene Reagents Reagents n-butylbromide sec-butylbromide

Q: What organic product is formed in the following reaction? (Note: here an ethyl group is not a…

Q: The alkyl chloride that will be the most reactive in a reaction of SN1

Q: Draw the structure of the major product of 2-bromo-4-methyl-3-hexyne + Li in NH3

A: Structure of 2-bromo-4-methyl-3-hexyne is as follows. Valency of carbon is four but here it is…

Q: 4. Complete the phrases with one or more of the following terms: Snl, Sn2, E1, E2. a) The reaction…

A: Points to remember: 1) SN1: Nucleophilic substitution reaction of first order SN2: Nucleophilic…

Q: Nucleophilic aromatic substitution involves the formation of a resonance-stabilized carbanion…

Q: In the addition reactions of alkynes, the reagents undergo transformation to form first. a. a…

Q: Which of the following is not true of SN₁ reactions? A. They are favored by nonpolar solvents. B.…

A: Here we are required to find the statement which is true for Unimolecular substitution reaction

Q: HBr

Q: The formation of a carbocation is the rate-determining step for an SN2 reaction. A. True B.…

A: Given statement: The formation of a carbocation is the rate-determining step for an SN2 reaction. We…

Q: 1. As we've seen, SN1/E1 reactions can be quite messy and can generate multiple products. Consider…

A: Alkyl halide gives elimination and substitution reactions. Both E1 and SN1 reactions proceed by the…

Q: The elimination reaction of butan-2-ol will produce butene and but-2-ene via mechanism O a. SN1 O b.…

Q: Demonstrate the results of the reactions between this alkyne and the various reagents. NaNH2…

A: Alkyne is most reactive among hydrocarbons because of the presence of two pie bonds which are quite…

Q: What alkenes are formed from attached alkyl halide by an E1 reaction? Use the Zaitsev rule to…

A: In an E1 elimination reaction, the more substituted alkene is formed as the major product.

Q: Draw the starting structure that would lead to this major product under these conditions. Select to…

Q: H3C N. Он H3C°

A: Given,

Q: Heck reactions take place with alkynes as well as alkenes. The following conversion involves an…

A: We have to draw the intermediate of the given Heck coupling reaction.

Q: The Stille reaction is similar to the Suzuki reaction. It replaces the alkenyl-organoboron compound…

A: Stille coupling: The Pd (0) catalyzed cross-coupling reaction which involves the use of aryl or…

Q: Which alkyl bromide(s) can form the alkene under E2 elimination conditions. Na CH;CH,OH Br Br. Br A…

Q: Provide a short answer for why the secondary alkyl halide is the major product versus the tertiary…

A: Note : tertiary radical is more stable. A kinetic product is formed via more stable intermediate at…

Q: CH3 CH2BR NBS hv

Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

The compound below undergo elimination reaction to produce 2 types of alkenes. Based on Zaitsev rule, what will be
the major product of this elimination?
ОН
O a. 2-methylpent-4-ene
O b. 4-methylpentene
O c. 4-methylpent-2-ene
d. methylpentene

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

Step 3

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 3 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

Supply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2
Rank these alkyl halides in order of increasing reactivity in an SN2 reaction
(1) Design the synthesis of: (a) CH3C≡CCH2CH3 from HC≡CH and appropriate alkyl halides. (b) (CH3)2CBrCH2CH3 from (CH3)2C=CHCH3
Show the SN2 mechanism in the reaction between (S) 2-bromobutane and iodide ion. Label the product and draw a enery diagram for this reaction.
(a) Draw a Kekulé structure that shows how the reactive positions of anthracene are the ends of a diene, appropriate for a Diels–Alder reaction.(b) The Diels–Alder reaction of anthracene with maleic anhydride is a common organic lab experiment. Predict the product of this Diels–Alder reaction.
Draw the major organic product of this E1 elimination reaction. Ignore byproducts.
Internal alkynes are able to selectively form one product when subjected to most reaction conditions. T or F Alkynes react with one equivalent of acid to create a carbocation for Markovnikov addition. T or F Alkynes react very similarly to alkenes. Understanding the mechanisms from chapter 12 will help understand the reaction pathways in chapter 13 where mechanisms are not explicitly drawn. T or F
Alkyl diazonium salts (shown below) are considered "super" leaving groups; a consequence of this is that they tend to be contact explosives What quailities make alkyl diazonium salts such excellent leaving groups?
Consider the following alkyl halides: - may react with NaI to give JKL? - an alkyl iodide that will give SN1 and E1 product? - has the highest boiling point? - most likely to give retention and inversion products in SN1 reaction? - most likely to give rearrangement product in SN1?
what is the starting material using Diekmann cyclization reaction