The following molecule has how many degrees of unsaturation?64 Using the rule of 13, what is a possible formula for M=113 (100%) on a mass spectrum?all of the above are possible molecular formulasCH130CH15N

Answered: Image /qna-images/answer/f18642b1-5205-478f-9e81-0b32f76f0210.jpg

Answered: The following molecule has how many…

Science

Chemistry

The following molecule has how many degrees of unsaturation? 6. 4 3

Living by Chemistry

2nd Edition

ISBN:9781464142314

Author:Angelica M. Stacy

Publisher:Angelica M. Stacy

ChapterU5: Fire: Energy , Thermodynamics, And Oxidation-reduction

Section: Chapter Questions

Problem 17RE

See similar textbooks

Related questions

Q: d) ОН

A: The most stable conformation of cyclohexane ring is called as chair conformation. The reason behind…

Q: SECH3 CH3 CH3 SECH3 CH3 H3C H3C H3C. `SECH3 SeCH3 HзC. SECH3 ČH3 CH3 ČH3 A SECH3 В C H3C CH3

A: The given molecule is: The molecule can be converted into various forms of its chair conformations.…

Q: Which of the following is the lowest energy conformer of the following compound looking down the…

A: 1St option is correct.

Q: 2) Draw the newman projection for each chair conformation of A and B (1 newman projection per chair…

A: The Newman projection for the chair conformations A and B have been described below. The structures…

Q: • Draw the chair conformations of the following compounds and determine which geometric isomer is…

Q: Cyclobutane is more stable molecule than cyclopropane, because... Select one: it has less angle…

A: Option D is correct Answer.

Q: NH2

A: Introduction: We have to calculate degree of unsaturation for the given molecule.

Q: Consider the following chair conformation of bromocyclohexane: н н H. Br H H H (a) Identify whether…

A: Cyclohexane exists in various conformations such as the chair, boat, half-boat, twisted, etc. Among…

Q: 3. Draw the chair conformer of cyclohexane. Label the axial hydrogens (Ha) and the equatoria…

A: Cyclohexane exist in chair form , which contain two types of hydrogen , axial hydrogens and…

Q: Rank the conformers of 1,2,4-trimethylcyclohexane in order of decreasing stability, putting the most…

A: The axial (a) and equatorial (e) position in a chain conformation of a cyclohexane ring can be…

Q: A Newman projection of methylcyclohexane is shown below. Identify the which atoms will provide…

Q: a. Draw Newman projections of the two conformers of cis-1,3-dimethylcyclohexane. b. Which of the…

Q: a. b.

A: Constitutional isomers have same molecular formula but have different bonding patterns.

Q: Draw a Newman projection formula for the most stable staggered conformation of 1,2-dibromoethane

Q: Draw a Newman projection of the structure in its highest potential energy staggered conformation in…

Q: a) b) F 3 * 2 Н. O O 2 2 3 CH3 3 Ō CI I configuration C2 configuration C3 2 3 configuration C2…

Q: 3. (20) Cyclohexane may go through ring-flipping as shown below. 5 (a) Draw both of the possible…

Q: Consider the following energy diagram for the compound z IV II III 0° 180° 360° C3-C4 Dihedral angle…

A: A question based on projection formula, which is to be accomplished.

Q: 4. A compound has two carbons each with the same set of four different substituents, but does not…

A: The carbon that is attached with the four different substituents is termed as chiral carbon or…

Q: 11. Draw the Newman projection of the alkane conformation shown below looking down the indicated C-C…

A: Newman projection: These are one of the ways to explain stereochemistry of alkanes. The…

Q: Chair Conformer = axial bond = equatorial bond Draw 1,2,3,4,5,6-hexachlorocyclohexane with a. all…

A: Given Name of structure = 1,2,3,4,5,6 -hexachlorocyclocyclohexane a) when all the chloro group is…

Q: please could they be answered and they aren't graded questions

A: Newman projection is utilized in alkane stereochemistry. Through Newman's projection, carbon atom…

Q: g. Draw two chair conformations of the following molecule and indicate which one is more stable. h.…

A: Here we have to write the chair conformation and predict the most stable conformation of the…

Q: a) b) 4. Assign the absolute configuration of all molecules. Draw the most stable conformer in…

A: Here priority order is Cl>F>carbon branch of other numbering carbon>H. First priority…

Q: Q2. Draw all possible Newman projections for the below structure by sighting along the indicated…

Q: Draw (2R,3S)-3-chloropentan-2-ol. Also, using Newman projections draw the least and most stable…

A: 1. Staggered conformations are more stable. In staggered some of the conformations are having 3…

Q: 2. Draw the two chair conformations for both cis- and trans-2-isopropylcyclohexanol (a planar form…

A: Here we have to write the more stable chair conformation of cis - 2-isopropylcyclohexanol and trans…

Q: In an eclipsed conformation of the Newman projection, the dihedral angle, which is an angle between…

A: Ans

Q: 3.Draw the most stable chair conformation for each of the following compounds (a)…

A: Chair conformation of cyclohexane is more stable.

Q: Draw every stereoisomer for 1-bromo-2-chloro-1,2-difluorocyclopentane. Use wedge-and-dash bonds for…

A: Please find your solution below : Stereoisomers are the compounds which have same composition but…

Q: Below are two conformers of trans-1-tert-butyl-3-methylcyclohexane. As shown in the equilibrium,…

A: Conformational isomers: The conformational isomers are formed by the rotation of a carbon-carbon…

Q: can this be explained please with full and understandable explanation

Q: a) b) F Н. O 2 2 2 3 3 CH3 3 3 O CI configuration C2 configuration C3 2 3 configuration C2…

Q: (b) (c) Draw the more stable chair conformation of each of the following compounds in which an…

A: In organic chemistry, Cyclohexane rings have different kind of conformations in which cyclohexane…

Q: A compound has a molecular formula of CyHg. How many unsaturations does this molecule have? 3 4. 6.…

A: Correct answer is 4. Degree of unsaturation = number of pie bonds + number of rings Degree of…

Q: Label the pair of compounds below as: a. identical b. stereoisomersc. constitutional isomers d.…

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: 6. Using Newman projections, draw each of the following molecules in its represented conformation…

Q: 4. Draw the correct MO diagram for the n-system of the following compound Energy

A: Given molecule is cyclopentadienyl anion.

Q: ght along the C2-C3 blond of 2-methylbutane: a)draw the newman projection of the most stable…

Q: true or false the more stable chair conformation of a substitued cyclohexane has the greater number…

A: In chair conformation the substituents can be placed at both equatorial and axial positions . But…

Q: Calculate the number of degrees of unsaturation for each molecular formula. a.C6H8 b.C40H56…

A: Since you have posted question with multiple subparts, we will solve first three subparts for you.…

Q: Draw both chair conformations of cyclohexane. Label the axial hydrogens a and the equitoral…

A: Given Name of Compound = Cyclohexane structure of both chair conformation = ?

Q: estion Draw the most stable conformation of ethylcyclohexane. Show every bond to hydrogen. Clearly…

A: The most stable conformation of a cyclohexane is chair form with all the substituent at axial or…

Q: Consider conformer X below and the result of its ring flip conforme conformer X Which of the…

A: In Compound X, All functional group in axial position so Compound X have 1,3-diaxial intraction with…

Q: 1.46 Draw the more stable chair conformation for each of the following disubstituted cyclohexanes.…

Q: a. Sketch the alignments of these groups through a 360° rotation by using the Newman Projections…

Q: 6. a. Draw both chair conformations for trans-1,2-dichlorocyclohexane. Label all unfavorable…

Q: 5.Draw the most stable conformer of each of the following ) Use Newman projections for straight…

A: a. anti form is most stable as it involves least streric repulsion between bulky methyl groups. b.…

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

100%

The following molecule has how many degrees of unsaturation?
6
4

Using the rule of 13, what is a possible formula for M=113 (100%) on a mass spectrum?
all of the above are possible molecular formulas
CH130
CH15N

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step 3

VIEW

Step by step

Solved in 3 steps with 3 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

The mass spectrum of bromine (Br2) consists of three peaks with the following characteristics: Mass (u) Relative Size 157.84 0.2534 159.84 0.5000 161.84 0.2466 How do you interpret these data?
The mass spectrum of CH3Cl is illustrated here. You know that carbon has two stable isotopes, and 13C with relative abundances of 98.9% and 1.1%, respectively, and chlorine has two isotopes, 35a and 37CI with abundances of 75.77% and 24.23%, respectively. (a) What molecular species gives rise to the lines at m/Z of 50 and 52? Why is the line at 52 about 1/3 the height of the line at 50? (b) What species might be responsible for the line at m/Z = 51?
(E) What does the number (+Z) at the center of each atom in Figure 1.1 represent, and whatnumber would you expect at the center of a representation of a bromine atom (Br)?
If the mass spectrum of a sample has a 7.7% M+1 peak compared to a 100% M+ peak, how many carbon atoms are we then likely to have in our chemical formula?
The highest mass peaks in the mass spectrum of Br2 occur at m/Z 158, 160, and 162. The ratio of intensities of these peaks is approximately 1:2:1. Bromine has two stable isotopes,79Br (50.7% abundance) and 81Br (49.3% abundance). question: What molecular species gives rise to each of these peaks? (Include the mass numbers of the isotopes in your answers.)
Questions 2: What is the principle that allows us to use a mass spectrometer to determine the intensity of a peak?* Higher molecular mass compounds are less volatile than lower molecular mass compounds. Cations of higher mass are deflected less by a magnetic field than cations of lower mass. Cations reaching the detector causes a current that is proportional to the size of these ion. O Larger çations takes longer to reach the detector. O All of these statements are correct.
What type of compounds/molecules can be detected using LC-MS and what mass range or molecular mass ranges can be detected using LC-MS?
What molecular ions will be present in a mass spectrum of 2-chloropropane ? ( HINT: 1. Calculate the molecular weights using each of the common isotopes of Cl. 2. Write down the molecular formula for 2-choloropropane with the isotopes of chlorine and then calculate the mass of molecular ion , m/z).
Bromine has two naturally occurring isotopes, 79Br , abundance 50.52%, and 81Br, abundance 49.48%. The most stable form of bromine under standard conditions is as the diatomic molecule, Br2 . In a mass spectrum of bromine, at what m/z values would you expect to see peaks and what would you expect the relative height of the peaks to be? What species would account for each peak? Explain.
In the mass spectrum of an unknown organic compound, the molecular ion had a relative abundance of 19.0 while the M+1 had a relative abundance of 1.5. Estimate the number of carbons in the molecule. 1 4 7 2 LO 5 8 carbons 3 6 9 X C
Consider the mass spectrometer shown in Figure 2.11. Determinewhether each of the following statements is true or false.If false, correct the statement to make it true: (a) The pathsof neutral (uncharged) atoms are not affected by the magnet(b) The height of each peak in the mass spectrum is inverselyproportional to the mass of that isotope.
Which mass spectrum would be best for determining the molecular mass and the chemical structure of the compond and provide reasons