Interpretation:
Thechemical formula and the structure for the given mass spectrum and
Concept introduction:
Mass spectrometry is the detection of ions on the basis of their weights and charges and their abundance.
Mass spectroscopy is a graph with the mass (
Molecular ions formed by EI mass spectrometry are high energy species. Cleavage of a single bond produces a cation and a radical. The Cation can be detected using positive ion mass spectrometry and since the radical is not charged, it will be undetected.
Chain branching or cleavage of a single bond at branch points will occur such that the carbocation formed is more stable.
Carbon-carbon bonds adjacent to atoms with unshared electron pair break readily to form carbocations which are stabilized due to resonance.
Nuclear magnetic resonance spectroscopy is a graph showing the characteristic energy absorption frequencies and intensities of a compound under a magnetic field.
Chemical shifts are the positions of signals along the x-axis in the nuclear magnetic spectroscopy. It gives an idea of how many different hydrogens are present in a given H-NMR for a particular compound.
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Organic Chemistry
- Spectra of an organic compound A are shown below. Compound A has empirical formula C2H4O. Using this information, the mass and infrared spectrum, deduce the molecular formula of A. A) 1,2-Dimethoxyethylene B) 1,4-Dioxane C) Butanoic acid D) Methyl propanoate E) 2-Butene-1,4-diolarrow_forwardPlease don't provide handwriting solutionarrow_forwardHere are proton NMR data for 1-bromopropane: Ha : triplet (2H) 3.32ppm; Hb : multiplet (2H)1.81ppm; Hc : triplet (3H) 0.93ppm. (Relative integrations shown in parentheses.) a. Through how many bonds can a hydrogen split another hydrogen? b. According to this splitting rule, does Ha split Hc ? c. Is your answer in part a) consistent with the multiplicity listed for peak clusters a and c? d. How many hydrogenssplit Hb ? e. Upon very close inspection of the proton NMR spectrum of 1-bromopropane, you wouldfind that peak cluster b has at least six peaks. Is this consistent with your answer in part d)? f. Speculate as to why any peak cluster with more than four peaks is listed simply as a"multiplet."arrow_forward
- The infrared spectrum of the compound with the mass spectrum shown below lacks any significant absorption above 3000 cm-1. There is a prominent peak near 1740 cm-1 and another strong peak near 1200 cm-1. Propose a structure consistent with the data.arrow_forwardFollowing is the mass spectrum of an unknown compound. The two highest peaks are at m/z 120 and 122. Suggest a structure for this compound. (Data from http://webbook.nist.gov/chemistry/.)arrow_forward1) Propose the structures for the following 1H and 13C NMR spectrum. b) Molecular Formula: C8H8O3 1H-NMR, CDCl3 Solvent, Molecular Formula: C8H8O3 13C-NMR, CDCl3 Solvent, Molecular Formula: C8H8O3 in the picturesarrow_forward
- 4. Deduce the structure of a compound with the molecular formular C8H10O that exhibits the following ¹H NMR and ¹³℃ NMR spectra. (6 pts) Proton NMR 22 7 Carbon NMR There are two. 160 unresolved lines at 130 ppm 140 120 5 Chemical Shift (ppm) 100 80 60 Chemical Shift (ppm) 40 3 20 2V 0arrow_forwardProvide the structure or SMILES of the compound with molecular formula C8H8O and correlates with the NMR shown in the imagearrow_forwardNeed some assistance with NMR question please! Thank you so much! Part 3B Set 2. Can 1H NMR spectroscopy be used to differentiate between the two compounds? Briefly explain why or why not. Predict the 1H NMR spectrum for each compound (include integration, multiplicity, and approximate chemical shift). Either draw the actual spectrum or put in a data table format.arrow_forward
- (II) Study this aromatic molecule and answer the following questions: Br H3 NO2 Br a) How many 'H-NMR signals this compound will show? B What will be the splitting (coupling) of H1, H2, and H3? H1 H2 H3 c) Which of the two hydrogens, Hl or H3 will show larger coupling, and which will show smaller coupling? Explain your answer: d) Draw the signal for H2:arrow_forwardThe mass spectrum of compound C, with a molecular formula C8H7BrO2 is shown below. 1.Draw the most likely ion fragment for the signals at m/z 155, 159, 183, and 185.Explain why these signals appear as pairs with almost similar intensities in the mass spectrum. 2.Identify and draw the structure of compound C.arrow_forwardPlease show work 1. Compound A has molecular formula C5H10O. It shows three signals in the 1H-NMR spectrum - a doublet of integral 6 at 1.1 ppm, a singlet of integral 3 at 2.14 ppm, and a quintet of integral 1 at 2.58 ppm. Suggest a structure for A and explain your reasoning.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning