7. (Chapter 15 - Q41a) Propose a structure for the compound that fits the following description. Ca0H14 7.18 5, (4H, broad singlet) 2.70 8 (4H, quartetJ =7 Hz) 1.20 5 (6H. triplet J =7 Hz) IR: 745 cm1 7(a) IR absorption indicate the compound is -disubstituted = 7(b) The name of the compound is

7. (Chapter 15 - Q41a) Propose a structure for the compound that fits the following description. Ca0H14 7.18 5, (4H, broad singlet) 2.70 8 (4H, quartetJ =7 Hz) 1.20 5 (6H. triplet J =7 Hz) IR: 745 cm1 7(a) IR absorption indicate the compound is -disubstituted = 7(b) The name of the compound is

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: A compound with formula C6H14O gave the following HNMR: 1.17 ppm, t, 3H 1.20 ppm, s , 9H 3.42 ppm,…

A: The spectroscopy technique of nuclear magnetic resonance (NMR) is extremely useful for the study of…

Q: Use the following spectroscopic data to work out the structure of an organic compound: Molecular…

A: :

Q: 3. Draw structures corresponding to the following IUPAC names: (a) Triethylamine (b)…

A: 3. Given IUPAC names: (a) Triethylamine (b) N-Methylaniline (c) Tetraethylammonium bromide (d)…

Q: A and B are isomeric dicarbonyl compounds of the molecular formula C5H&O2. The 'H NMR spectrum of A…

A: So by given data the structure we can interpre8 as follows:

Q: A chemist was trying to synthesize compound C over the course of two steps, butafter the first step…

A: Step 1: Step 2:

Q: Give IUPAC names for the following alkanes, and convert each drawing into a skeletal structure. 3-20…

Q: If possible please answer both questions thank you!

A: a. Isobutylamine b. Butanal

Q: The IR spectrum of compound X (C8H15OCl) shows an absorption at 1800cm-1. Which functional groups…

A: Molecular formula C8H15OCl

Q: Compound B of molecular formula C9H19N shows a noteworthy infrared absorption at 3300 cm-1. Its…

A: Interpretation: To determine the structure of a compound B with molecular formula C9H19N which shows…

Q: Give two names for the following compound:

A: Naming of 3 membered ring with oxygen containing heterocyclic compound Two methods 1. The…

Q: Compound A (C11H23Br) is a secondary alkyl halide. On being heated with a solution of sodium…

A: We will use the given information to find out the compounds associated with these observations. It…

Q: Ide a structure for the mpound with the 113NO using the given ihformation. 360, 3280 cm-1 (doublet);…

Q: here are several isomeric alkanes of molecular formula C6H14.Two of these exhibit the following…

A: Isomer A δ (ppm) Splitting pattern No of Hydrogen 0.84 doublet (d) 12 H 1.39 septet 2H…

Q: phosphorus reagent is required for this n? PPh3 (B) (C) PPh3 H PPh3 (D) PPh3

A: Wittig reaction is the formation of olefins from the aldehyde and ketone when treated with…

Q: Propose a structure for the compound that fits the following description. C10H14 7.18 δ, (4H,…

A: The study of an interaction between the electromagnetic radiation and matter is known as…

Q: 1,3,5,7-Cyclooctatetraene, CgHg, is an unusual hydrocarbon in that it reacts with exactly 2…

A: 1,3,5,7-Cyclooctatraene(COT) is an unsaturated derivative of cyclooctane, with the formula C88

Q: IR: 1600, 2880, 3020. Further data based on IR: Compound underwent reaction... IR of precursor to…

A: Formula= C10H14O2

Q: Propose a structure consistent with following spectral data for a compound C8H18O2

A: Solution-

Q: Draw the structure of a compound with the formula C5H10O2 (along with the reasons of choosing it)…

Q: Compound B has molecular formula C9H10. The IR spectrum is shown below. The 1H-NMR spectrum shows a…

A: Nuclear Magnetic Resonance or NMR spectra are commonly used in the prediction of any unknown organic…

Q: Propose a structure that fits the description: a nitrile, C3H5N.

A: A nitrile is an organic compound that contains a cyano (-CN) functional group.

Q: Propose a structure consistent with following spectral data for mpound C8H18O2: IR: 3350 cm-1 'H…

Q: 3. A student synthesized Compound 1 (following). To purity the compound, he extracted it into…

A: The objective of the question is to understand the chemical transformation of Compound 1 (CH2CO2H)…

Q: 5. (Chapter 15 - Q41b) Propose a structure for the compound that fits the following description.…

Q: A compound of mass 149 has the following elemental analysis: C = 80.48%, H=10.13%, N=9,39%. The IR,…

A: Let's summarize some spectroscopic techniques organic chemistry :Infrared Spectroscopy…

Q: Provide a structure for the given compound. UV spectrum: Amax = 272 nm (e = 39500); EI mass…

A: The objective of the question is to determine the structure of a compound using the given…

Q: In an attempt to synthesize compound C through a two-step process, a chemist discovered after…

A: Step 1:• In this reaction, Firstly base abstract the acidic proton to forms enolate ion which…

Q: (c) Compound C has a molecular formula of C6H14O. The IR spectrum shows strong absorption bands at…

Q: (d) Ozonolysis of 3,4-dimethyl-3-hexene gives compound D. (1) Write the reaction step for the…

Q: Give the compounds with the following spectral data. a. C8H8O3 IR: 3500 cm' to 2500 cm, 1688 cm!…

A: The inspecting of an unknown compound by its molecular formula is done by calculating the index of…

Q: Compound B of molecular formula C9H19N shows a noteworthy infrared absorption at 3300 cm-1. Its…

A: Molecular formula of the compound = C9H19N IR spectrum: 3300 cm-1 1H-NMR: δ 1.0 (6H), 1.1 (12H), 1.4…

Q: Compound p,c6h14O does not react w/sodium metal,doesn't discharge the color of Br2 in ccl4, the…

Q: 2. Draw the structure of the products that will be formed when aniline reacts with nitrous acid at 5…

A: When aniline reacts with nitrous acid at 5°C then benzene diazonium salt form. Benzene diazonium…

Q: organic compound B with formula C6H14O has the following: IR Spectroscopy 2974 cm-1, 1080 cm-1…

Q: Propose a structure for D (molecular formula C,H9CIO2) consistent with the given spectroscopic data.…

Concept explainers

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.

Question

7. (Chapter 15 - Q41a) Propose a structure for the compound that fits the following
description.
Ca0H14
7.18 5, (4H, broad singlet)
2.70 8 (4H, quartetJ =7 Hz)
1.20 5 (6H. triplet J =7 Hz)
IR: 745 cm1
7(a) IR absorption indicate the compound is -disubstituted =
7(b) The name of the compound is

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

Step 3

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 3 steps with 2 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

24) Which of the following reagents would you use as the basis for a simple chemical test that would distinguish between ethylbenzene and styrene? (a) Nal/acetone (b) Br2/CCl4 (c) NaOH/H2O (d) NaBH4/CH3OH (e) HBr/H2O ethyl benzene styrene
Treatment of 1,3,6-cyclononatriene (Compound 1), or its dimethyl derivative (Compound 2), with potassium amide (KNH₂) in liquid ammonia results in the formation of anion 1a or 2a, respectively (J. Am. Chem. Soc. 1973, 95, 3437-3438): 9 15.85a 2 6 3 4 5 Compound 1 (R=H) Compound 2 (R=CH3) * You answer is incorrect. KNH₂ KNH₂ 1a (anion) 2a (anion) Of the following, which is NOT one of the four resonance structures of 1a?
The proton NMR spectrum of a compound with formula C8H14O2 is shown. TheDEPT experimental results are tabulated. The infrared spectrum showsmedium-sized bands at 3055, 2960, 2875, and 1660 cm-1and strong bands at1725 and 1185 cm-1. Draw the structure of this compound and assign thecarbon peaks.
Aspirin, or 2-acetoxybenzoic acid, (C9H8O4) is often synthesised from salicylic acid.(i) Sketch and discuss any changes in the number of possible structural conformations ofaspirin relative to those of salicylic acid. (ii) Re-draw the structure predicted to be the lowest energy conformation of aspirin,indicating any expected stabilising and destabilising interactions. Justify your choice.
An amine of unknown structure contains one nitrogen and nine carbon atoms. The 13C-NMR spectrum shows only five signals, all between 20 and 60 ppm. Three cycles of Hofmann elimination sequence [(1) CH3I; (2) Ag2O, H3O; (3) heat] give trimethylamine and 1,4,8-nonatriene. Propose a structural formula for the amine.
28(f) Give name(s) of major organic product(s) of the following reaction. H2N-NH2 КОН
Identify which of the following functional groups appear in the molecule daumone. (Note that some of the functional groups in daumone will not be listed as an answer option) Daumone has been isolated and is found to extend life in worms. When Caenorhabditis elegans worms find their environment crowded and inhospitable, they hibernate until food becomes available, effectively extending their life span. Daumone is the compound that has been found to be responsible for this hibernation. HO но. OH Daumone O Ester
Name the following compounds A and B. How could you distinguish these two molecules by using 1H NMR and IR techniques? Propose an analytical technique to determine the iron content of these compounds. Calculate the mass percentages of C and H of compound B (C: 12.01 g/mol; H: 1.008 g/mol; Fe: 55.845 g/mol).
1. There are several isomeric alkanes of molecular formula C6H14.Two of these exhibit the following 1H-NMR spectra. Propose a structure for each of the isomers. Isomer A: δ = 0.84 (d, 12 H), 1.39 (septet, 2H) ppm Isomer B: δ = 0.84 (t, 3 H), 0.86 (s, 9H), 1.22 (q, 2H) ppm
In the 1HNMR spectrum for 4-bromobenzyl alcohol, assign the various resonances to thehydrogen nuclei responsible for them.