**Instruction:**Draw the structure of (Z)-3-methylhept-3-ene. Be sure the stereochemistry is drawn clearly.**Toolbar Details:**- **Select, Draw, Rings, More, Erase:** Options for creating and modifying structures.- **Drawing Tools:** Includes bond creation and manipulation tools. - **Single Bond:** Creates a single bond between atoms. - **Double Bond:** Creates a double bond, necessary for alkenes. - **Triple Bond:** Creates a triple bond when needed.- **Element Selection:** - **C:** Carbon atom - **H:** Hydrogen atom**Additional Features:**- **Undo/Redo Arrows:** Allows reversing or repeating the last action.- **Zoom Tools:** For adjusting the view of the drawing.**Explanation:**- **Alkene Structure:** (Z)-3-methylhept-3-ene features a double bond (alkene) at the third carbon in a seven-carbon chain (hept-).- **Stereochemistry:** The (Z) configuration indicates that the higher priority groups attached to the double-bonded carbons are on the same side.- **Methyl Group:** A methyl group is attached to the third carbon of the main chain.

An alkene is named as E- alkene when the substituents with same priority present on opposite side of…

Answered: Draw the structure of…

Science

Chemistry

Draw the structure of (Z)-3-methylhept-3-ene. Be sure the stereochemistry is drawn clearly.

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: Determine which C of the double bond is more substituted C(1) or C(2) for each of the following…

A: The alkene containing a large number of alkyl groups connected to the double bonded carbon atom is…

Q: (a) 4-Bromo-2-hexene (Z), (R) isomer name: (Z), (S) isomer name: (E), (R) isomer name: (E), (S)…

A: Given is organic compound .The name of given compound is,4-Bromo-2-hexene

Q: Provide the structure of (Z)-1-chloro-1-fluoro-1-butene.

A: The structure is given in below picture

Q: Draw tetrahedral representations of the following molecules: (a) (S)-2-Chlorobutane (b)…

A: In tetrahedral representation two groups are in plane and one group is at weidge and other is at…

Q: 1. Name the following molecules according to the IUPAC nomenclature system. Indicate stereochemistry…

A: The name of the given compound are provided according to IUPAC Nominclature in attach image. ,

Q: а-pinene When a-pinene reacts with 1. ВН3; 2. На О2, NaOH, Н2О 4 possible cis,trans isomers can be…

Q: Draw the structure of the stated product and choose the conditions that would result in the product…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Draw the structure of (Z)‑5,6‑dimethylhept‑4‑en‑1‑yne.

A: The structure of an organic compound is written in the following steps: Determine the number of…

Q: What is the IUPAC name for this compound?

A: 1. Select the principle carbon chain 2. Numbering 3. Naming (prefix + word root + suffix)

Q: Draw a skeletal (line-bond) structure of (R)-4-ethyloctane. Use a dash or wedge bond to indicate…

Q: Draw the following molecules. Clearly show the stereochemistry in your drawings! (3R)-3-fluoroctane…

A: A stereo formula can be represented in two dimensions using the Fischer projection or Fischer…

Q: Using skeletal formulas and where appropriate showing the correct stereochemistry and bond geometry…

A: Given that, the names of the compounds are:(a) oct-6-under-3-one(b)…

Q: Draw the skeletal (line-bond) structure of (R)-2-methylpentan-3-ol. Use a dash of wedge bond to…

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: Give a name to the following enantiomer: CI H CH₂CH3 CH 3 Select one: O (R)-3-chlorobutane O…

A: The given compound is shown below.We have to give the IUPAC name of the given compound.

Q: This question is based on the five compounds (A-E) given below. (A) CH;-CH=CH-CH3 (B) (C) CHCI=CHBR…

Q: CI CH₂ CH R CHS A Compound A CI CH CH base R "CH Compound A where R is: Cha CH₂ CH₂ CH₂ CH₂ R R "CH₂…

A: Axial group due to 1,3-diaxial interaction decreases the stability of cyclohexane derivatives. So,…

Q: Draw the structure 3-Chloro-4-ethy actore 3- bromo-1 chloro-4-ethyl actore 2-bromo-4-ethylhexane…

A: IUPAC stands for International Union of Pure and Applied Chemistry. IUPAC helps to draw the…

Q: Draw a structural formula for 2,3,3-trimethylhexanoic acid.

A: Given , Molecule : 2,3,3 -trimethyl hexanoic acidObjective : Darw the structural formula of 2,3,3…

Q: is question is based on the five compounds (A-E) given CH;-CH=CH-CH3 ) CH;-C(CI)(CH;)-CH2-CH3 )…

A: Esters have fruity smell or aroma due to their volatile nature caused by their chemical composition.

Q: Please draw out the structure of compounds A-D. Four compounds A, B, C and D have same molecular…

A: To deduce the structures of compounds A-D.

Question

**Instruction:**

Draw the structure of (Z)-3-methylhept-3-ene. Be sure the stereochemistry is drawn clearly.

**Toolbar Details:**

- **Select, Draw, Rings, More, Erase:** Options for creating and modifying structures.
- **Drawing Tools:** Includes bond creation and manipulation tools.
- **Single Bond:** Creates a single bond between atoms.
- **Double Bond:** Creates a double bond, necessary for alkenes.
- **Triple Bond:** Creates a triple bond when needed.
- **Element Selection:**
- **C:** Carbon atom
- **H:** Hydrogen atom

**Additional Features:**

- **Undo/Redo Arrows:** Allows reversing or repeating the last action.
- **Zoom Tools:** For adjusting the view of the drawing.

**Explanation:**

- **Alkene Structure:** (Z)-3-methylhept-3-ene features a double bond (alkene) at the third carbon in a seven-carbon chain (hept-).
- **Stereochemistry:** The (Z) configuration indicates that the higher priority groups attached to the double-bonded carbons are on the same side.
- **Methyl Group:** A methyl group is attached to the third carbon of the main chain.

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

(a) (R)-1,1,2-trimethylcyclohexane, label each structure you have drawn as chiral or achiral.
Is C-O ester of 3-chloro-4’-methoxychalcone conjugated (talking about the H3CO attatched to the benzene ring)? Can you explain your answer?
Alkenes can be converted to alcohols by hydroboration-oxidation. (a) Draw the structure of the alcohol or alcohols formed in the reaction sequence. Clearly indicate stereochemistry by drawing a wedged bond, a dashed bond and two in-plane bonds per each chiral carbon. Draw hydrogen atoms that are connected to wedge-and-dash bonds.(b) Characterize the product or products of the reactions. Be sure to draw hydrogens on oxygen, where applicable. Select Draw Rings More Erase H 1. B,H§, diglyme (a) 2. H2O2, HO", H2O
Draw the organic product(s) of the following reactions, and include carbon dioxide if it is produced. KMNO4 / H3O* CH3CH2CH2-C=C-H • You do not have to consider stereochemistry. • If a compound is formed more than once, add another sketcher and draw it again. • Draw carbon dioxide in its own sketcher if it is produced. Separate multiple products using the + sign from the drop-down menu. • If no reaction occurs, draw the organic starting material.
Draw the following molecule, don't forget stereochemistry : (E)-5-ethyl-5-methylhept-3-ene
Draw the skeletal line-bond structure of (R)-4-isopropoxyoctane. Include a dash or wedge bond to indicate stereochemistry of substituents.
Draw structures for (R)-3-(4-ethylhexyl)cyclobutene and (E)-5-(bromomethyl)dec-5-ene.
4. Draw all possible stereoisomers of the following compounds. Assign the appropriate absolute (R/S) or geometric (E/Z) configuration to each of the stereoisomers (or double bonds) and label pairs enantiomers, diastereomers and meso compounds. (a) CH3CHBRCHOHCH3 (c) CH3CH=C(Br)CH=CHCI (e) CH3CH₂CHOHCHOHCH2CH3 (g) OH НО... CI (h) H3C Br (b) CH3CHBRCHBRCH ₂Br (d) CH3CH(C6H5)CHOHCH3 (f) CH₂(OH)CH2-CH(OH)CH=CHOH CH3 (1) Br HS Br
The two alkenes below react with HI at different rates. CH3CH=CHCH3 and CH₂=CH₂ Draw the structural formula of the MAJOR product formed by the alkene having the HIGHER reaction rate. • 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. TAYY [ ] در ChemDoodle Ⓡ