Propose a structure for the compound that fits the following description. C10H14 7.18 δ, (4H, broad singlet) 2.70 δ (4H, quartet J = 7 Hz) 1.20 δ (6H. triplet J = 7 Hz) IR: 745 cm-1 7(a) IR absorption indicate the compound is .........-disubstituted = 7(b) The name of the compound is =

Propose a structure for the compound that fits the following description. C10H14 7.18 δ, (4H, broad singlet) 2.70 δ (4H, quartet J = 7 Hz) 1.20 δ (6H. triplet J = 7 Hz) IR: 745 cm-1 7(a) IR absorption indicate the compound is .........-disubstituted = 7(b) The name of the compound is =

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter21: Benzene And The Concept Of Aromaticity

Section: Chapter Questions

Problem 21.26P: Compound I (C11H14O2) is insoluble in water, aqueous acid, and aqueous NaHCO3, but dissolves readily...

See similar textbooks

Related questions

Q: Amantadine is effective in preventing infections caused by the influenza A virus and in treating…

Q: 160 °C + 24h

Q: Write the products of the following sequences of reactions. Refer to your reaction roadmap to see…

Q: Compound X, C7H14 undergo hydration to form Y which is optically active. X reacts with cold alkane…

Q: 9) Provide a structure of an isomer that has the molecular formula CSH12N2 and fits the criteria…

A: Isomers are the compounds that have the same molecular formula but different structural formulas. A…

Q: Q5.) Two isomeric aromatic compounds X and Y have the following percentage composition by lmass! C =…

Q: A dibromide loses only one bromine when it reacts with sodium hydroxide. The dibromide forms toluene…

A: Given that, A dibromide loses only one bromine when it reacts with sodium hydroxide. The dibromide…

Q: Depending on the nature of substituent X, the structure below might expel a leaving group, X', to…

Q: On being heated with a solution of sodium ethoxide in ethanol, compound A (C7H15Br) yielded a…

A: In the first reaction, the elimination reaction results in the formation of alkene from alkyl…

Q: 7. The following SN2 reaction yields a product with the given empirical formula. Suggest a structure…

Q: a. NABH4 then H3o+ b. PBr3 c. Mg in dry ether, then CH2=O, then H30* d. Dess-Martin Periodinane e.…

A: The question is based on the concepts of Organic reactions. we have been given certain options. we…

Q: CHE2613/101/0/2022 3.2 The reaction of methylpropene with HBr, under radical conditions, gives bve…

A: Free radical takes place when homolysis cleavage takes place.

Q: How many monocholrinated products including stereoisomers would you predict to form from the…

Q: This question concerns the following nitrogen- containing compounds. CH2NH2 20 NH2 ÇONH2 P. CH3 CH3…

Q: 12. Based on the reaction scheme below, deduce and name structures A, B and C. H,, Pd A KMNO, В…

A: Ans

Q: 1. The sex attractant for the common housefly is a hydrocarbon with the molecular formula C23H46. On…

A: The molecular formula of the sex attractant for the common housefly is C23H46. First we have to…

Q: 3. Acetone, CH3(C=0)CH3, is known to all biologists because of its usefulness as a solvent and…

A: DBE of 1,1,3,3,5,5-hexamethyl trioxane = (C+1)+N/2-H/2-X/2 = (9+1)-18/2 = 10-9 = 1 When three…

Q: Propose structure(s) for the compound and give the physical properties, chemical properties, and…

A: The degree of unsaturation for the given compound, having a formula of C9H10O, is 5. Thus, one…

Q: Select from the list the most suitable reagents to carry out the transformations. Compounds with…

A: The selectivity of the reactions are as follows: B2H6 in presence of water selectively attaches the…

Q: A compound C4H11N is known from its reactivity andspectroscopic properties to have no hydrogen…

A: Structural formula: The chemical formula in which the bonds between them and all the atoms of the…

Q: Compounds Y and Z are isomers with the molecular formula C10H12O. The IR spectrum of each compound…

Q: Compound A, C 10H 18O, undergoes reaction with dilute H 2SO 4 at 50 °C to yield a mixture of two…

A: Given, Chemical formula of A is C10H18O. It reacts with H2SO4 at 500C and forms two alkene with…

Q: Chemistry Treatment of this keto-aldehyde with KOH gives a compound C7H100 with the spectroscopic…

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: Compound A, C 10H 18O, undergoes reaction with dilute H 2SO 4 at 50 °C to yield a mixture of two…

A: The organic compound can be nucleophilic (rich in electron density), or electrophilic…

Q: 11. The following diagram represents a synthesis which begins with bromoethane. (i) (iii) C2HGO (C)…

A: The compound D is an ester formed by the alcohol C and the carboxylic acid B.

Q: 13. Complete with stereolabels, give the IUPAC name of compound i, below: 14. Complete with…

A: Since we only answer 1 question in case of multiple question, we’ll answer the first question as the…

Q: (b) Compound C has the molecular formula of C;H12. The IR spectrum shows the important absorption…

Q: Please find the open chemical structure of the compound. Please indicate your comments on IR, 1H-NMR…

A: The analysis suggest the presence of hydroxyl and amine group attached on aromatic ring.

Q: Compound A (C 7H 11Br) is treated with magnesium in ether to give B (C 7H 11MgBr), which reacts…

A: Organic reactions:

Q: Reaction of acetic acid, CH3CO2H, with isotopically labeled CH318OH and catalytic sulfuric acid…

A: The reaction of an acid with alcohol is known as the esterification reaction.

Q: 1. In the reactions involving the three isomeric alcohols with the formula C4H9OH, describe what…

A: The reactivity of an alcohol is dependent upon the attachment of their functional hydroxyl group.…

Q: Compound X is optically inactive and has the formula C 16H 16Br 2. On treatment with strong base, X…

A: When alkyl halide is treated with a base, elimination reaction can occur. The elimination can either…

Q: Treating 1-methylcyclohexene with H30* would yield primarily which of these? HO II II но, IV a " b…

A: We have to predict the primary product of given reaction.

Q: for trans-1.2-dichlorocyo 3. The structure below is Formeterol, a long-acting b-adrenergic agonist…

A: Redraw the structure and label all the functional groups--

Q: Complete the following reaction by supplying the product. If more than one product is predicted give…

A: The electrons rich species which carry either negative charge or lone pair of electrons are…

Q: A dibromide loses only one bromine when it reacts with sodium hydroxide. The dibromide forms toluene…

A: Given that, A dibromide loses only one bromine when it reacts with sodium hydroxide. The dibromide…

Q: A compound A, C7H12, was found to be optically active. On catalytic reduction over platinum…

A: Alkynes are organic compounds containing carbon and hydrogen atoms. In alkynes, there is a presence…

Q: Compound X has molecular formula C5H10. In the presence of a metal catalyst, compound X reacts with…

A: Metal/ H2 reagent generally use for hydrogenation . So this will convert to alkene to alkane. And…

Q: What are the names of the compound A, B, C, D, E, F, G & H. Hence suggest structures for compound C…

Q: 8. There is a compound C1,H16 which has been proved to have double bond and isopropyl group. The…

A: Hydrogenation: When unsaturated double bond is reduced by the hydrogen is called hydrogenation. Or a…

Q: Are the compound names below representative of prochiral or not prochiral molecules? Label them…

A: In stereochemistry, prochiral molecules are those that can be converted from achiral to chiral in a…

Q: Compound A (C7H11Br) is treated with magnesium in ether to give B (C7H11MgBr), which reacts…

A: Structure A is alkyl halide which undergoes Grignard reaction to give product B, which on deuterated…

Q: Nitriles, R-CN, undergo a hydrolysis reaction when heated with aqueous acid. What is the structure…

A: Hydration reaction is the reaction in which unsaturation is removed by the addition of a water…

Q: Draw the structure resulting from a reaction of: 1. diborane (B₂H6), followed by 2. alkaline…

Q: 13. Draw the structure of the compound described below Hydroboration-oxidation of an alkene, C,H12,…

Q: diastereomer gives the E alkene, and the other gives the Z alkene. Which diastereomer gives the Z…

A: When same periority present same side then z-alkene and if same periority present opposite side…

Q: An optically active monoterpene (compound A) with molecular formula C10H18O undergoes catalytic…

Concept explainers

Analyzing Infrared Spectra

The electromagnetic radiation or frequency is classified into radio-waves, micro-waves, infrared, visible, ultraviolet, X-rays and gamma rays. The infrared spectra emission refers to the portion between the visible and the microwave areas of electromagnetic spectrum. This spectral area is usually divided into three parts, near infrared (14,290 – 4000 cm-1), mid infrared (4000 – 400 cm-1), and far infrared (700 – 200 cm-1), respectively. The number set is the number of the wave (cm-1).

IR Spectrum Of Cyclohexanone

It is the analysis of the structure of cyclohexaone using IR data interpretation.

IR Spectrum Of Anisole

Interpretation of anisole using IR spectrum obtained from IR analysis.

IR Spectroscopy

Infrared (IR) or vibrational spectroscopy is a method used for analyzing the particle's vibratory transformations. This is one of the very popular spectroscopic approaches employed by inorganic as well as organic laboratories because it is helpful in evaluating and distinguishing the frameworks of the molecules. The infra-red spectroscopy process or procedure is carried out using a tool called an infrared spectrometer to obtain an infrared spectral (or spectrophotometer).

Question

Propose a structure for the compound that fits the following description.

C₁₀H₁₄

7.18 δ, (4H, broad singlet)

2.70 δ (4H, quartet J = 7 Hz)

1.20 δ (6H. triplet J = 7 Hz)

IR: 745 cm^-1

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 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 solution of acetone [(CH3)2C=O] in ethanol (CH3CH2OH) in the presence of a trace of acid was allowed to stand for several days, and a new compound of molecular formula C7H16O2 was formed. The IR spectrum showed only one major peak in the functional group region around 3000 cm−1, and the 1H NMR spectrum is given here. What is the structure of the product?
Compounds B and C are isomers with molecular formula C5H9BrO2. The 1H NMR spectrum of compounds B and C are shown below. The IR spectrum corresponding to compound B showed strong absorption bands at 1739, 1225, and 1158 cm-1, while the spectrum corresponding to compound C have strong bands at 1735, 1237, and 1182 cm-1. 1.Based on the information provided, determine the structure of compounds B and C. 2.Assign all peaks in 1H NMR spectrum of compounds B and C.
Compound B of molecular formula C9H19N shows a noteworthy infrared absorption at 3300 cm-1. Its 1H-NMR spectrum shows three singlets – δ 1.0 (6H), 1.1 (12H), 1.4 (1H) ppm. Its 13C-NMR spectrum has four signals – δ 25, 28, 41, 64 ppm. Suggest a structure for this compound. Please show work.
Following are IR and 1H-NMR spectra of compound D. The mass spectrum of compound D shows a molecular ion peak at m/z 136, a base peak at m/z 107, and other prominent peaks at m/z 118 and 59. Q.) Propose structural formulas for ions in the mass spectrum at m/z 118, 107, and 59.
Compounds Y and Z are isomers with the molecular formula C10H12O. The IR spectrum of each compound shows a strong absorption band near 1710 cm−1 . The 1H NMR spectra of Y and Z are given below. Propose structures for Y and Z.
Propose a structure for the compound that fits the following description. C10H14 7.0 δ, (4H, broad singlet) 2.85 δ (1H, septet J = 8 Hz) 1.20 δ (6H, doublet J = 8 Hz) 2.28 δ (3H, singlet) IR: 825 cm-1 5(a) Degree of the unsaturation of this compound is= , 5(b) Two peaks at 2.85 δ and 1.20 δ indicate that the compound has .......... group = 4(c) A peak at 2.28 δ indicates that the compound has ............. group= 4(d) IR absorption indicates the compound is .........-disubstituted = 4(e) The name of the compound is =
A compound with the molecular formula C6H11BrO2 shows an intense band at 1739 cm-1 in the IR spectrum. The mass spectrum shows signals at m/z = 194 and 196 (about 1:1 intensity); 149 and 151 (about 1:1 intensity); 115; 121 and 123 (about 1:1 intensity); 166 and 168 (about 1:1 intensity); and 29. Suggest a reasonable structure for this compound that is consistent with this data.
Compound B of molecular formula C9H19N shows a noteworthy infrared absorption at 3300 cm-1. Its 1H-NMR spectrum shows three singlets – δ 1.0 (6H), 1.1 (12H), 1.4 (1H) ppm. Its 13C-NMR spectrum has four signals – δ 25, 28, 41, 64 ppm. Suggest a structure for this compound.
A compound of formula C6H10O2 shows only two absorptions in the proton NMR: a singlet at 2.67 ppm and a singlet at2.15 ppm. These absorptions have areas in the ratio 2:3. The IR spectrum shows a strong absorption at 1708 cm-1. Proposea structure for this compound.
Compound I (C11H14O2) is insoluble in water, aqueous acid, and aqueous NaHCO3, but dissolves readily in 10% Na2CO3 and 10% NaOH. When these alkaline solutions are acidified with 10% HCl, compound I is recovered unchanged. Given this information and its 1H-NMR spectrum, deduce the structure of compound I.
Ketones undergo a reduction when treated with sodium borohydride, NaBH4. What is the structure of the compound produced by reaction of 2-butanone with NaBH4 if it has an IR absorption at 3400 cm-1 and M+=74 in the mass spectrum?
The following sequence of steps converts (R)-2-octanol to (S)-2-octanol. Propose structural formulas for intermediates A and B, specify the configuration of each, and account for the inversion of configuration in this sequence.