MASTERING CHEMISTRY:THE CENTRAL SCIENCE
13th Edition
ISBN: 9781269712538
Author: Brown
Publisher: PEARSON
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Chapter 1, Problem 10E
Interpretation Introduction
To determine:
The steps to convert the speed of sound into miles per hour.
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1. Calculate the accurate monoisotopic mass (using all 1H, 12C, 14N, 160 and 35CI) for your product using the table in
your lab manual. Don't include the Cl, since you should only have [M+H]*. Compare this to the value you see on
the LC-MS printout. How much different are they?
2. There are four isotopic peaks for the [M+H]* ion at m/z 240, 241, 242 and 243. For one point of extra credit,
explain what each of these is and why they are present.
3. There is a fragment ion at m/z 184. For one point of extra credit, identify this fragment and confirm by
calculating the accurate monoisotopic mass.
4. The UV spectrum is also at the bottom of your printout. For one point of extra credit, look up the UV spectrum
of bupropion on Google Images and compare to your spectrum. Do they match? Cite your source.
5. For most of you, there will be a second chromatographic peak whose m/z is 74 (to a round number). For one
point of extra credit, see if you can identify this molecule as well and confirm by…
Please draw, not just describe!
can you draw each step on a piece of a paper please this is very confusing to me
Chapter 1 Solutions
MASTERING CHEMISTRY:THE CENTRAL SCIENCE
Ch. 1.2 - Which of the following is the correct description...Ch. 1.2 - Prob. 1.1.2PECh. 1.5 - Which of the following numbers in your personal...Ch. 1.5 - Practice Exercise 2 The back inside cover of the...Ch. 1.5 - Practice Exercise 1 An object is determined to...Ch. 1.5 - Practice Exercise 2 How many significant figures...Ch. 1.5 - Ellen recently purchased a new hybrid car and...Ch. 1.5 - Practice Exercise 2 It takes 10.5 s for a sprinter...Ch. 1.5 - Prob. 1.5.1PECh. 1.5 - Prob. 1.5.2PE
Ch. 1.6 - Practice Exercise 2 By using a conversion factor...Ch. 1.6 - Practice Exercise 1 Fabiola, who lives in Mexico...Ch. 1.6 - Prob. 1.7.1PECh. 1.6 - Practice Exercise 2 A car travels 28 mi per gallon...Ch. 1.6 - Practice Exercise 2 The surface area of Earth is...Ch. 1.6 - Practice Exercise 1 Composite decking is a...Ch. 1.6 - Prob. 1.9.1PECh. 1.6 - Practice Exercise 2 If the mass of the container...Ch. 1.6 - Practice Exercise 1 Which of the following is the...Ch. 1.6 - Aspirin is composed of 60.0% carbon, 4.5%...Ch. 1.6 - Practice Exercise 1 Which of the following weights...Ch. 1.6 - Practice Exercise 2 How many picometers are there...Ch. 1.6 - Practice Exercise 1 Using Wolfram Alpha...Ch. 1.6 - Practice Exercise 2 Ethylene glycol, the major...Ch. 1.6 - Prob. 1.13.1PECh. 1.6 - Practice Exercise 2 Calculate the density of a...Ch. 1 - The reaction between reactant A (blue spheres) and...Ch. 1 - Prob. 2ECh. 1 - Describe the separation method(s) involved in...Ch. 1 - Prob. 4ECh. 1 - Prob. 5ECh. 1 - Prob. 6ECh. 1 - Prob. 7ECh. 1 - 2447 What are the molecular and empirical formulas...Ch. 1 - When you convert units, how do you decide which...Ch. 1 - Prob. 10ECh. 1 - 2-60 The most common charge associated with...Ch. 1 - Prob. 12ECh. 1 -
2.84 Consider the following organic substances:...Ch. 1 -
2.96 Gallium (Ga) consists of two naturally...Ch. 1 -
2.108 Cyclopropane is an interesting hydrocarbon....Ch. 1 - Write a balanced equation for (a) solid...Ch. 1 - Calculate the molar mass of Ca(NO3)2Ch. 1 - Prob. 18ECh. 1 - Imagine you are working on ways to improve the...Ch. 1 - A key step in balancing chemical equations is...Ch. 1 - a. The characteristic odor of pineapple is due to...Ch. 1 - The complete combustion of octane, Cngs, a...Ch. 1 - Prob. 23ECh. 1 - Prob. 24ECh. 1 -
4.53 Write balanced molecular and net ionic...Ch. 1 - Prob. 26ECh. 1 - Prob. 27ECh. 1 - Prob. 28ECh. 1 -
4.101 Hard water contains Ca2+ , Mg2 + , and Fe2+...Ch. 1 - Prob. 30ECh. 1 - Prob. 31ECh. 1 - Prob. 32ECh. 1 - Imagine that you are climbing a mountain. Is the...Ch. 1 - A gas is confined to a cylinder under constant...Ch. 1 -
5.100 An aluminum can of a soft drink is placed...Ch. 1 - The hydrocarbons acetylene (C2H2) and benzene...Ch. 1 - The precipitation reaction between AgNO3(aq) and...Ch. 1 - Consider the following three moving objects: a...Ch. 1 - The speed of sound in dry air at 20°C is 343 m/s...Ch. 1 - Prob. 40ECh. 1 - Calculate the energy of a photon of...Ch. 1 - Using Heisenberg's uncertainty principle,...Ch. 1 - Prob. 43ECh. 1 - The following do not represent valid ground-state...Ch. 1 - Prob. 45ECh. 1 - Prob. 46ECh. 1 - Arrange the following atoms and ions in order of...Ch. 1 - Prob. 48ECh. 1 - Prob. 49ECh. 1 - The distance from Grand Rapids, Michigan, to...Ch. 1 - Prob. 51ECh. 1 - Prob. 52ECh. 1 - Prob. 53ECh. 1 - Prob. 54ECh. 1 - Prob. 55ECh. 1 - Which of the these molecules has a Lewis structure...Ch. 1 - Prob. 57ECh. 1 - Write the electron configuration for the element...Ch. 1 - (a) Classify each of the following as a pure...Ch. 1 - Prob. 60AECh. 1 - Prob. 61AECh. 1 - Prob. 62AECh. 1 - Prob. 63AECh. 1 - Prob. 64AECh. 1 - Prob. 65AECh. 1 - Prob. 66AECh. 1 - Prob. 67AECh. 1 - Prob. 68AECh. 1 - Ethyl acetate. C4H802, is a fragrant substance...Ch. 1 - Prob. 70AECh. 1 - The iodine bromide molecule, IBr, is an...Ch. 1 - Prob. 72AECh. 1 - Prob. 73AECh. 1 - Prob. 74AECh. 1 - Prob. 75AECh. 1 - Prob. 76AECh. 1 - Prob. 77AECh. 1 -
10.12 The graph below shows the change in...Ch. 1 - Prob. 79AECh. 1 - Prob. 80AECh. 1 - Prob. 81AECh. 1 - Prob. 82AECh. 1 - Prob. 83AECh. 1 - Prob. 84AECh. 1 - Prob. 85AECh. 1 - Prob. 86AECh. 1 - Prob. 87AECh. 1 - Prob. 88AE
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- > Can the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? esc ? A O O •If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. • If your answer is no, check the box under the drawing area instead. olo 18 Ar Explanation Check BB Click and drag to start drawing a structure. 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Accessibilityarrow_forwardName the structurearrow_forward> For each pair of substrates below, choose the one that will react faster in a substitution reaction, assuming that: 1. the rate of substitution doesn't depend on nucleophile concentration and 2. the products are a roughly 50/50 mixture of enantiomers. Substrate A Substrate B Faster Rate X CI (Choose one) (Choose one) CI Br Explanation Check Br (Choose one) C 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy A F10arrow_forward
- How to draw this mechanism for the foloowing reaction in the foto. thank youarrow_forwardPredict the major products of the following organic reaction: Some important notes: CN A? • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. No reaction. Explanation Check Click and drag to start drawing a structure. 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Centerarrow_forwardDraw the major product of the following reaction. Do not draw inorganic byproducts. H3PO4 OHarrow_forward
- Predict the major products of this organic reaction: HBr (1 equiv) Δ ? Some important notes: • Draw the major product, or products, of this reaction in the drawing area below. • You can draw the products in any arrangement you like. • Pay careful attention to the reaction conditions, and only include the major products. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. • Note that there is only 1 equivalent of HBr reactant, so you need not consider the case of multiple additions. Explanation Check X ©2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacyarrow_forwardFor the structure below, draw the resonance structure that is indicated by the curved arrow(s). Be sure to include formal charges. :ÖH Modify the second structure given to draw the new resonance structure. Include lone pairs and charges in your structure. Use the + and - tools to add/remove charges to an atom, and use the single bond tool to add/remove double bonds.arrow_forwardUsing the table of Reactants and Products provided in the Hints section, provide the major product (with the correct stereochemistry when applicable) for questions below by selecting the letter that corresponds to the exact chemical structures for the possible product. OH conc Hydrochloric acid 40°C Temp A/arrow_forward
- Using arrows to designate the flow of electrons, complete the reaction below and provide a detailed mechanism for the formation of the product OH conc Hydrochloric acid 40°C Temp All chemical structures should be hand drawn on a piece of paper Paragraph BI UAE +varrow_forwarddraw out the following structures plesearrow_forwardDraw everything on a piece of paper outlining the synthesis from acetaldehyde to 2 cyclopentene carboxaldehyde using carbon based reagants with 3 carbons or fewers. Here is the attached image.arrow_forward
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