2) A compound having molecular formula C3H60 gave the following spectral data:( 1 ) υν : λax 292 nm, εman 21(ii) IR: 2720 cm1 (w) and 1738 cm(s) . Deduce the structure of the compound.

Answered: 2) A compound having molecular formula…

2) A compound having molecular formula C3H60 gave the following spectral data: (i) UV: Amax 292 nm, ɛmax 21 (ii) IR: 2720 cm1 (w) and 1738 cm(s) . Deduce the structure of the compound.

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: Analysis of a sweet-smelling, neutral compound of carbon, hydrogen and oxygen produced the following…

A: Signals of proton NMR shows the number of equivalent protons present in the organic compound.

Q: Identify this compound with molecular formula C9H10O IR peak at 1742 cm-^1,H nmr data (ppm) at…

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: 1) They were given a mysterious chemical by ASP Rinuprasad, coded as Compound X, which was believed…

A: Note: compound is having aldehyde functional group. ( 2800 cm-1, 2700 cm-1 aldehyde C-H stretch and…

Q: A compound has a molecular formula of C8H8O The following spectra (1H NMR, Carbon 13 NMR, IR was…

A: IR spectra is the spectra that uses the IR radiation to excite the molecule where the IR spectrum is…

Q: Which of the following compounds is consistent with the ¹H NMR spectrum shown below? 7 1H dd (A) 1H…

Q: Treatment of compound D with LiAlH4 followed by H2O forms compound E. D shows a molecular ion in its…

Q: what is is the structure of a compound of molecular formula c 10 h 14 o 2 that shows a strong ir…

Q: The 1H-NMR spectrum of compound B,C7H14O , consists of the following signals: δ 0.9 (t, 6H), 1.6…

A: The objective of this question is to find the structure of a compound based on given HNMR spectra.

Q: Based on the information provided, determine the structures of compounds. (b) Assign all peaks in 1…

A: Structure of unknown organic compound based on the given spectral data is Nitropropane.

Q: 3000 * TRANSMITTANCE 6CCC LS62 1248

A: Provided molecular formula of compound=C4H10O Broad ir peak at =3339 cm-1 Provided 6H doublet at…

Q: Draw the structure of the molecule and upload it here. Molecular Formula: C,H₁002 -1 FTIR: Strong…

Q: An experimental data set has been acquired to determine the structure of an unknown compound. (a)…

A: We need to calculate molecular formula of the given compound and determine functional group.

Q: Briefly describe what it consists of and what information can be obtained in the characterization of…

A: Given : a) Infrared spectroscopy (IR)b) Mass spectrometry (MS)c) Proton nuclear magnetic resonance…

Q: An unknown compound has a molecular formula of C4H₂O. Its IR spectrum shows prominent absorptions at…

A: We will do all sorts of possible analysis from the given data and try to find out the structure of…

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

A: Nuclear magnetic resonance which is more precisely known as NMR is used to determine the local…

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

Q: (g) Compounds A and B _having identical molecular formula C¸H30 have the following : 13C signals at…

A: Using the given information structure of compounds A and B having the same molecular formula…

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: (b) An organic compound molecular formula C12H3 Br2. Identify has the the compound using the…

A: Site of unsaturation - 8

Q: Deduce the structure of compound A C9H1002 , Amax= 253 cm-1 , IR bands,3035, 2960, 2870, 1680, 1610,…

Q: the following observations tros

A: As you have mentioned that three and fourth are to be solved, so I have solved this third and fourth…

Q: On the basis of the molecular formula, 1H NMR data, and IR data provided, propose a consistent…

A: The question is based on the concept of organic spectroscopy. We need to analyse the spectral data…

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

Q: (b) One isomer of dimethoxybenzoic acid has 1H NMR spectrum dµ (ppm) 3.85 (6H, s), 6.63 (1H, t, J 2…

A: Step 1: The detailed explanation along with the spliting pattern for the presence of specific two…

Q: Compound A has molecular formula C5H8Br4 but shows only one singlet in the 1H-NMR spectrum. Suggest…

A: The compound is showing only single peak in H-NMR, so all the hydrogen present in the compound must…

Q: 1H NMR spectra and formulas

A: Given data, C9H10O The structure of the given proton NMR spectra can be identified as

Q: Propose a structure for an organic compound with molecular for mula Ca HH04 given the pollowing…

A: There are 3signal in 1H NMR spectra Triplet (6H ) , singlet (3H) , quadret (4H) Degree of…

Q: A compound A of mass 114 has the following elemental analysis: C = 63.14%, H=8.83%. The IR, 1H NMR…

A: Proton-NMR spectroscopy is mainly used for the identification of complete structure of the orgnanic…

Q: 2.0 2.5 1.e

A: The structure given the 1H NMR spectra has to be suggested and each of the compounds for the…

Q: (a) Compound A has molecular formula C5H10O. It shows three signals in the 1H-NMR spectrum - a…

A: The Ir spectra tells us about the functional groups present in that molecule. proton and carbon-13…

Concept explainers

NMR Spectroscopy

NMR stands for Nuclear Magnetic Resonance in which the study of different molecules is done based on the interaction of radiofrequency electromagnetic radiations with the nuclei of molecules placed in a strong magnetic field. A precise study of spectra of visible light and all bands of electromagnetic radiation is called spectroscopy.

Question

2) A compound having molecular formula C3H60 gave the following spectral data:
( 1 ) υν : λax 292 nm, εman 21
(ii) IR: 2720 cm1 (w) and 1738 cm(s) . Deduce the structure of the compound.

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 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

An organic compound B with formula C6H14O has the following: IR Spectroscopy 2974 cm-1, 1080 cm-1 Mass Spectrometry 102 (M+), 87, 73 1H NMR Spectroscopy Eight signals at δ 1.10 (d, 3H), 1.13 (dd, 3H), 1.14 (dd, 3H), 1.59 (ddq, 1H), 1.60 (ddq, 1H), 3.19 (ddq, 1H), 3.51 (dq, 1H), 3.50 (dq, 1H). Compound B is obtained by the reaction of compound A with NaH followed by CH3CH2Br. The stereochemistry of A is "S" Using this information, deduce a plausible structure for Compound A with correct stereochemistry.
The 1H-NMR spectrum of Compound C shows five signals – δ 2.38 (1H, dt), 2.72 (1H, dt), 5.34 (1H, t), 5.49 (2H, ddd), 6.27 (2H, dd) ppm. Its 13C-NMR spectrum has four signals – δ 26, 58, 127, 129 ppm. In the compound’s mass spectrum, the M+1 peak appears at m/z = 115. An M+2 peak, whose intensity is roughly one-third that of the M+1 peak, also appears. Suggest a structure for this compound.
(asap plz
The treatment of (CH3)2C=CHCH2Br with H2O forms B (molecular formulaC5H10O) as one of the products. Determine the structure of B from its 1H NMR and IR spectra.
A molecule of the molecular formula C5H11Br gives rise to the NMR spectrum below. When reacted with NaOH and water, it forms a product which by NMR has 2 protons 1H at 5.4 ppm and 1H at 5.5 ppm each having a J coupling of 17 Hz. (other protons also present) The product also has an IR stretch at 1550 cm1. Provide the structures of the starting material (1 pt) and product (2 pts) NaOH H20 C5H1,Br 6H triplet 4H quintet 1H quintet 10 8 7 6. 4 3 1 HSP-06-347 ppm
the compound B C23H46,a sex attractant of the common housefly,gave two products Ch3(cH2)12COOH and CH3(CH2)7COOH. Based on this information, suggest the likely structures of B
Use the 1H NMR and IR data to determine the structure of attachedcompound.
Treatment of 2-methylpropanenitrile [(CH3)2CHCN] withCH3CH2CH2MgBr, followed by aqueous acid, affords compound V, whichhas molecular formula C7H14O. V has a strong absorption in its IRspectrum at 1713 cm−1, and gives the following 1H NMR data: 0.91(triplet, 3 H), 1.09 (doublet, 6 H), 1.6 (multiplet, 2 H), 2.43 (triplet, 2 H), and2.60 (septet, 1 H) ppm. What is the structure of V?
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.
Deduce the structure of compound C.
Compound A with the molecular formula of C12H15ClO₂ has the following ¹H-NMR spectral data: Chemical shift (ppm) 1.38 2.08 2.83 3.51 4.36 7.27 7.96 ¹H-NMR Spectrum Multiplicity triplet quintet triplet triplet quartet doublet doublet Integration Ratio 3 2 2 2 2 2 2 The IR spectrum of A exhibits a signal at 1738 cm-¹. Based on the above information, determine the structure of compound A with a detailed explanation.
Predict the theoretical number of different NMR signals produced by each compound,and give approximate chemical shifts. Point out any diastereotopic relationships.(a) 2-bromobutane