/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 34 Which compound can show position... [FREE SOLUTION] | 91影视

91影视

Log out

Learning Materials

Features

Discover

Chapter 2: Problem 34

Which compound can show position isomerism? (A) Butene (B) Allene (C) Propene (D) Isobutene

Short Answer

Expert verified
The compound that can show position isomerism is (A) Butene.

Step by step solution

01

Analyse each compound

: Let's analyze each compound and see if they have the potential for position isomerism. (A) Butene (\(C_4H_8\)) is an alkene with a double bond between two carbon atoms. There are two possible position isomers for butene: 1-butene and 2-butene. (B) Allene (\(C_3H_4\)) is an alkene with two double bonds. In this compound, the central carbon atom is attached to two other carbon atoms by double bonds. As there is only one way to arrange this, allene cannot show position isomerism. (C) Propene (\(C_3H_6\)) is an alkene with one double bond between carbon atoms. With only three carbon atoms, there's only one possible position for the double bond (between the first and second carbon), so propene cannot show position isomerism. (D) Isobutene (\(C_4H_8\)) is an alkene with one double bond and a branched structure. There is only one way to arrange the double bond and the branching, so isobutene cannot show position isomerism.
02

Identify the compound with position isomerism

: Now, we can see that only (A) Butene has different possible positions for the functional group (double bond), and hence it can show position isomerism. So, the answer is (A) Butene.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91影视!

Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Position Isomerism
Position isomerism is a type of structural isomerism observed in organic compounds, particularly where there is a variation in the position of the functional group on the parent chain. In simpler terms, it occurs when the basic carbon skeleton of a molecule remains the same but the position of a particular group or substituent changes.

For example, in alkenes, a functional group of interest is the double bond. When the location of this double bond changes along the chain, each variant is called a position isomer. Position isomerism is significant because even though isomers have the same molecular formula, their chemical and physical properties can differ greatly due to the positioning of the functional groups.
Butene
Butene, also known as butylene, is a molecule with the molecular formula \(C_4H_8\) and is a member of the alkene family. Alkenes are hydrocarbons that contain at least one carbon-to-carbon double bond, and the position of this double bond can vary.

There are different isomers of butene, such as 1-butene and 2-butene. In 1-butene, the double bond is located at the end of the molecule, between the first and second carbon atoms. In 2-butene, the double bond shifts one position along the chain, between the second and third carbon atoms. Each isomer exhibits unique properties, and recognizing their structural differences is crucial for understanding their reactivity and functionality in various chemical reactions.
Alkenes
Alkenes are a class of hydrocarbons characterized by the presence of at least one carbon-to-carbon double bond, denoted as \(C=C\). This double bond is the functional group of alkenes, and it is responsible for their unique chemical properties. Alkenes have the general formula \(C_nH_{2n}\), indicating that they have two fewer hydrogen atoms than the corresponding alkanes.

The most essential aspect of alkenes, apart from being unsaturated hydrocarbons, is their ability to undergo addition reactions due to the double bond. These reactions include hydrogenation, halogenation, and others, making alkenes highly reactive and useful in the chemical industry for producing a wide range of products, including plastics, detergents, and pharmaceuticals.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

In which reaction, the observed rotation of mixture slowly decreases and finally approaches to zero? (A) \((+)-1\)-chloro- 1 -phenyl ethane \(+\mathrm{SbCl}_{5}\) (B) (-)-2-methyl butanal in alkaline condition (C) (+)-2-butanol in acidic condition

How many esters are possible with molecular formula \(\mathrm{C}_{4} \mathrm{H}_{8} \mathrm{O}_{2} ?\) (A) 2 (B) 3 (C) 4 (D) 5

Find the total number of optically active dichlorides of diphenyl methane.

Choose the incorrect statement about ephedrine and its enantiomer (A) The molecular weights of both enantiomers are the same. (B) The boiling point of both enantiomers is different. (C) Both enantiomers rotate the PPL by the same number of degree but in opposite direction. (D) Absolute configuration of shown enantiomer is ( \(1 \mathrm{R}, 2 \mathrm{~S}\) ).

Incorrect set of \(X\) and \(Y\) respectively when compound is an isomer of isobutane is (A) \(-\mathrm{CH}_{2} \mathrm{CH}_{3},-\mathrm{H}\) (B) \(-\mathrm{CH}_{3},-\mathrm{CH}_{3}\) (C) \(-\mathrm{H},-\mathrm{CH}_{2} \mathrm{CH}_{3}\) (D) \(-\mathrm{H},-\mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{3}\)
See all solutions

Recommended explanations on Chemistry Textbooks

Inorganic Chemistry

Read Explanation

Kinetics

Read Explanation

Chemical Analysis

Read Explanation

The Earths Atmosphere

Read Explanation

Making Measurements

Read Explanation

Organic Chemistry

Read Explanation
View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.