p-Fluoroanisole reacts with sulfur trioxide and sulfuric acid. Draw the major product of this substitution reaction; if applicable, minimize formal charges via expanded octets. Assume 1 equivalent of reagents is used.

p-Fluoroanisole reacts with sulfur trioxide and sulfuric acid. Draw the major product of this substitution reaction; if applicable, minimize formal charges via expanded octets. Assume 1 equivalent of reagents is used.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Related questions

Q: 2 methylbutene react with Hbr to give

A: The reaction of HBr to an alkene is referred to as a regioselective reaction, in which one direction…

Q: Compound A and compound B are constitutional isomers with molecular formula C3H₂Cl. Treatment of…

A: The ratio of the product of substitution reaction to the elimination reaction depends on the…

Q: 2-Methylpropene reacts with cold aqueous sulfuric acid to give A(C4H10O). Treatment of A with sodium…

A: Given1. 2-Methylpropene2. Cold aqueous sulphuric acid3. Compound A is 4. sodium metal in anhydrous…

Q: Give the IUPAC names for the following compounds. aryl cations. Example: ethyl cation. Be sure to…

A: Rules for the IUPAC name of organic compounds:1. Identify the longest carbon chain.2. Identify all…

Q: HgSO4, H₂O H₂SO4 CF3COOOH

Q: lydroxylation of E-2-pentene with osmium tetroxide yields a different product than the ame reaction…

Q: i) Give the IUPAC name of this molecule. ii) Outline the mechanism of this reaction. Your mechanism…

A: IUPAC nomenclature of alkenes : Select the longest chain of alkene containing both the carbons of…

Q: Please draw the structure of (E,4S)-4-methyl-2-hexene

Q: C.

A: Tertiary (3°) carbonation is more stable than secondary (2° ) because 3° carbonation is more…

Q: Compounds with more than one hydroxyl group can react with thionyl chloride differently from simple…

A: One hydroxyl group reacts with thionyl chloride and oxidises alcohol to corresponding aldehyde or…

Q: Draw the products of the following reactions. Remember Markovnikov's rule (if applicable). (a)…

A: Alkene can be defined as an organic compound containing double bond and alkyne contain triple bonds.

Q: Complete the following reaction by drawing the structure of the major product(s) expected. CH3 HCI…

A: The answer to the following question is-

Q: draw the products that could be formed in a reactionof benzene with 2hno3 in the presence of…

A: Benzene reacts with nitric acid in presence of concentrated sulfuric acid to form nitrobenzene ,…

Q: 5A Explain which of the following statements are true and which are false. i. N,N'-dicyclohexylurea…

A: The objective of the question is to determine the veracity of the given statements related to…

Q: 2. Limonene is a compound found in orange oil and lemon oil. When limonene is treated with excess…

A: The primary ingredient in citrus fruit peel oil is limonene, a colourless liquid aliphatic…

Q: Can the following alkanes (A and B) be synthesized from the same alkene via a hydrogenation…

Q: Maleic anhydride may be prepared using two routes: Oxidation of benzene: Oxidation of but-1-ene: 22…

A: Given:Preparation of maleic anhydride via two routes with 65% and 55% yield.To determine:(a) (i)…

Q: [Review Topics] [References] Compound X has the formula C3H16- X reacts with one molar equivalent of…

A: Molecular formula = C8H16

Q: 2. Please draw out structure of the following compounds. 1) 2,3-Methyl-1,4-pentadiene 2)…

Q: Benzene and alkyl-substituted benzenes can be hydroxylated by reaction with H₂O₂ in the presence of…

A: The objective of this question is to propose the mechanism for the hydroxylation if benzene.

Q: 2. Draw the structures of the products that would result from the following reactions. Ph Ph. (a)…

A: The detailed recation of these pericyclic reaction is given below.

Q: What would be the major product obtained from the reaction of Br2 with 1-butene if the reaction were…

A: This is bromination reaction. Alkene react with bromine to give dibromo compound

Q: Consider the nucleophilic substitution reaction between 3-chloro-3-methylpentane and the hydroxide…

A: This reaction proceeds in two steps. The first step is the removal of the leaving group to form a…

Q: Draw the products of the following reactions. Remember Markovnikov's rule (if applicable). (a)…

A: The structures for the given reactions are:

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

p-Fluoroanisole reacts with sulfur trioxide and sulfuric acid. Draw the major product of this substitution reaction; if
applicable, minimize formal charges via expanded octets. Assume 1 equivalent of reagents is used.
SO3
H2SO4
Modify the starting material to draw the major product.
Select
Draw
Rings
More
CH 0 S F
Erase

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: Write the objective

VIEW

Step 2: Explanation

VIEW

Solution

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 3 steps with 4 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

Intermidiates and reagents of the following two final products from a Acetylene Note: the final products are different reactions but use the same starting material.
Draw the alkene that would react with the reagent given to account for the product formed. ? + + H₂O **** H₂S04 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. CH3 CH3 CHCCH3 | | OH CH3 +1
The SN2 reaction is an example of a nucleophilic substitution reaction. Draw the structure of the two reactants and the mechanism of the reaction. The reaction is 1-bromo-3-ethylpentane reacts with cyclohexanol under basic conditions.
Nitration of an aromatic ring involves an electrophilic substitution reaction. Draw the structure of the electrophile that is attacked by the aromatic ring and the intermediate formed after attachment of the electrophile to the ring. Be sure to show formal charges.
INSTRUCTIONS: Choose from the options A-E and explain briefly by illustrations the chemistry behind each answer. Preamble: A reaction flask contains a 2-bromopentane in an ethanolic solution of sodium ethoxide at room temperature and results in the formation of two olefinic products. Predict the products that would be formed from such a reaction a)1-pentene (80%) and 2-pentene (20%)B)1-pentene (20%) and 2-pentene (80 %)C)1-pentene (50 %) and 2-pentene (50 %)D)1-pentene (0 %) and 2-pentene (100 %)E)1-pentene (100 %) and 2-pentene (0 %) What reaction pathway is followed by the reaction above?a)E2 dehydrohalogenation B)E1 dehydrohalogenationC)SN1 dehydrohalogenationD)SN2 dehydrohalogenation A mixture of E1 and E2 pathways What is responsible for the formation of different products (major and minor).A)The different activated complex involved in the mechanism. B)Bimolecular nuclephilic substitution reaction C)Bimolecular Elimination reaction D)The presence of sodium ethoxideE)The…
МЕСНANISMS 1,2-epoxy-1-methylcyclopentane undergoes both acid-catalyzed and base-catalyzed opening of the epoxide ring to form two different products. > Using ethanol as the solvent and an appropriate acid, show the steps in the acid catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s). > Using ethanol as the solvent and an appropriate base, show the steps in the base- catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s). 1,2-epoxy-1-methylcyclopentane CH3
5B In the following reactions, mixtures of alkenes and ethyl ethers are formed. Draw their structures. Explain which is or are likely to be the main product(s) in each reaction. In case of formation of two isomers of alkenes, explain which is formed in greater proportion CH3 CH3 H3C-C H -Br CH3 EtOH
Which of the following statements is incorrect? O One product of the ozonolysis of 1-butyne is carbon dioxide. O Hydration of 2-butyne would give one unique ketone as a product. O The hydrogenation of 1-butene releases less heat than the hydrogenation of trans-2-butene. The epoxidation of an alkene using MCPBA is stereospecific. A common source of carbon dioxide is dry ice.