**Exercise: Naming Alkenes****Task:** Provide an IUPAC name for each of the compounds shown below. **Note:** Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.---**Compound 1:**- **Structure Explanation:** - The compound consists of a carbon-carbon double bond (C=C) at the center. - Attached to the double-bonded carbons are two hydrogen atoms on one carbon and a substituent chain, CHCH(CH₃)₂, along with another CH₃, on the other carbon.- **Naming Guidelines:** - Determine the longest carbon chain that includes the double bond. - Identify substituents and their positions. - Apply (E)/(Z) nomenclature if applicable.---**Compound 2:**- **Structure Explanation:** - The compound features a central carbon-carbon double bond (C=C). - The left carbon of the double bond carries two methyl groups (CH₃ and CH₃CH). - The right carbon of the double bond has a hydrogen atom and a methyl group (H and CH₃). - **Naming Guidelines:** - Identify the main carbon chain across the double bond. - Identify and position substituents correctly. - Apply (E)/(Z) nomenclature if it affects the molecular geometry.---Utilize these guidelines to accurately name each compound according to IUPAC standards. The image depicts two structural formulas of alkenes:1. The first structure shows an alkene with the molecular formula likely being C8H16. It features a central double bond, with an ethyl group (CH3CH2-) and a butyl group (CH2CH2CH3) attached to one side, and a hydrogen (H) and a methyl group (CH3) bonded to the other carbon of the double bond.2. The second structure shows another alkene with a molecular formula likely being C7H14. In this structure, there is a pentyl group (CH3CH2C-) with a branching methyl group, and an ethylene group (CH2) bonded to it.Below each structure, there are placeholders that appear to be designed for the names or labels of these alkene compounds. These are empty and enclosed within rectangular borders, suggesting spaces for identification or categorization of the chemical structures shown above them.

Answered: Image /qna-images/answer/94b0b66a-1ada-43dc-9ff6-b47cc26b3983.jpg

Answered: rovide an IUPAC name for each of the…

rovide an IUPAC name for each of the compounds shown. Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only.

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

Similar questions

pls help
How to assign E & Z configurations and name tetra-substituted alkenes? And How do you determine tetra-substituted, mono-substituted, di-substituted?
N|ON|OU|G fic|Gb| app.101edu.co Maps YouTube 0³ A ℗ 2 F2 W S CO X G d B 2|GD|QC|GA Question 13 of 31 Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is ignored. 1- 3- 2- 6- 4- 5- iso tert- di tri sec- cyclo pent hept non 99 MacBook Air # 3 > 0 80 F3 E D $ S4 Aav F4 R F 0, % 5 F F5 T G 6 Y & 7 H F7 U * 00 8 J DII F8 W G 1 CS UONEE 9 K F9 ) O O F10 L Done P Gri J F11 + (
Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) CH3 CH3 ČH3 Br, CH3 C=C H H2C-CH2
Name (IUPAC) these following bicyclic compounds, find their molecular structure and find the constitutional isomers. i) ii) iii) о iv)
How many isomers (structural, geometric, and stereo) have the formula C5H10, and have "cyclo" in their name? (i.e. they contain a ring) 4 06 07 5
Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) CH3 CH3CH₂CH CI C=C CI CH3 -CH₂CH3 CH₂CH3
What is natural gas? a. a gas that forms from decaying vegetation b. a mixture of hydrocarbon gases, mostly methane c. a gas that forms naturally from coal d. naturally occurring hydrogen
Thank u
1,3-Cyclohexadiene the monoepoxide and sodium acetate as the major products: cis + reacts with peroxyacetic acid in the presence of sodium carbonate, giving racemic trans Na₂CO3 H3C OOH CH₂Cl₂, 0 °C 75% yield Select all terms that describe the monoepoxide (which has a cis-cyclic alkene): + H3C ONa+ (۵۰) <10% yield
`
[Review Topics] [References] An alkene having the molecular formula C6H10 is treated sequentially with ozone (03) and zinc/acetic acid to give the product/s shown. CH3CCH,CH,CH2CH Draw a structural formula for the alkene. • 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. P. aste Ado ChemDoodle Previous Next