
Chemistry
12th Edition
ISBN: 9780078021510
Author: Raymond Chang Dr., Kenneth Goldsby Professor
Publisher: McGraw-Hill Education
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Textbook Question
Chapter 10.7, Problem 1RC
Estimate the bond enthalpy (kJ/mol) of the
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1. Predict the organic product(s) of the following reactions. Assume excess of reagents unless
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There are 48 pairs of students in the following table. Each pair has quantitatively determined the mass of taurine in a 250 mL can of the popular energy drink marketed as “Munster” using High Performance Liquid Chromatography (HPLC). The class results are presented below:
QUESTION: Summarise and report these results including an indication of measurement uncertainty.
In both calculation samples calculate if an outlier is present, max value, number of samples, mean, standard deviation, g (suspect), g (critical) and t (critical).
Mass of Taurine (mg)
Mass of Taurine (mg)
(Table continued)
152.01
152.23
151.87
151.45
154.11
152.64
152.98
153.24
152.88
151.45
153.49
152.48
150.68
152.33
151.52
153.63
152.48
151.68
153.17
153.40
153.77
153.67
152.34
153.16
152.57
153.02
152.86
151.50
151.23
152.57
152.72
151.54
146.47
152.38
152.44
152.54
152.53
152.54
151.32…
Indicate the rate expressions for reactions that have order 0, 1, and 2.
Chapter 10 Solutions
Chemistry
Ch. 10.1 - Use the VSEPR model to predict the geometry of (a)...Ch. 10.1 - Which of the following geometries has a greater...Ch. 10.2 - Does the AlCl3 molecule have a dipole moment?Ch. 10.2 - Carbon dioxide has a linear geometry and is...Ch. 10.3 - Compare the Lewis theory and the valence bond...Ch. 10.4 - Determine the hybridization state of the...Ch. 10.4 - Describe the hybridization state of Se in SeF6.Ch. 10.4 - What is the hybridization of Xe in XeF4Ch. 10.5 - Describe the bonding in the hydrogen cyanide...Ch. 10.5 - Which of the following pairs of atomic orbitals on...
Ch. 10.6 - One way to account for the fact that an O2...Ch. 10.7 - Estimate the bond enthalpy (kJ/mol) of the H2+...Ch. 10.7 - Which of the following species has a longer bond...Ch. 10.8 - Describe the bonding in the nitrate ion (NO3) in...Ch. 10 - How is the geometry of a molecule defined and why...Ch. 10 - Sketch the shape of a linear triatomic molecule, a...Ch. 10 - How many atoms are directly bonded to the central...Ch. 10 - Discuss the basic features of the VSEPR model....Ch. 10 - Prob. 10.5QPCh. 10 - Prob. 10.6QPCh. 10 - Predict the geometries of the following species...Ch. 10 - Predict the geometries of the following species:...Ch. 10 - Predict the geometry of the following molecules...Ch. 10 - Predict the geometry of the following molecules...Ch. 10 - Predict the geometry of the following molecules...Ch. 10 - Predict the geometries of the following ions: (a)...Ch. 10 - Describe the geometry around each of the three...Ch. 10 - Which of the following species are tetrahedral?...Ch. 10 - Prob. 10.15QPCh. 10 - Prob. 10.16QPCh. 10 - Prob. 10.17QPCh. 10 - The bonds in beryllium hydride (BeH2) molecules...Ch. 10 - Referring to Table 10.3, arrange the following...Ch. 10 - The dipole moments of the hydrogen halides...Ch. 10 - List the following molecules in order of...Ch. 10 - Does the molecule OCS have a higher or lower...Ch. 10 - Which of the molecules (a) or (b) has a higher...Ch. 10 - Prob. 10.24QPCh. 10 - What is valence bond theory? How does it differ...Ch. 10 - Use valence bond theory to explain the bonding in...Ch. 10 - Prob. 10.27QPCh. 10 - Prob. 10.28QPCh. 10 - What is the angle between the following two hybrid...Ch. 10 - How would you distinguish between a sigma bond and...Ch. 10 - Describe the bonding scheme of the AsH3 molecule...Ch. 10 - What is the hybridization state of Si in SiH4 and...Ch. 10 - Describe the change in hybridization (if any) of...Ch. 10 - Consider the reaction BF3+NH3F3BNH3 Describe the...Ch. 10 - What hybrid orbitals are used by nitrogen atoms in...Ch. 10 - What are the hybrid orbitals of the carbon atoms...Ch. 10 - Specify which hybrid orbitals are used by carbon...Ch. 10 - Prob. 10.38QPCh. 10 - The allene molecule H2CCCH2 is linear (the three C...Ch. 10 - Prob. 10.40QPCh. 10 - How many sigma bonds and pi bonds are there in...Ch. 10 - How many pi bonds and sigma bonds are there in the...Ch. 10 - Give the formula of a cation comprised of iodine...Ch. 10 - Give the formula of an anion comprised of iodine...Ch. 10 - What is molecular orbital theory? How does it...Ch. 10 - Sketch the shapes of the following molecular...Ch. 10 - 10.47 Compare the Lewis theory, valence bond...Ch. 10 - Explain the significance of bond order. Can bond...Ch. 10 - Explain in molecular orbital terms the changes in...Ch. 10 - The formation of H2 from two H atoms is an...Ch. 10 - Prob. 10.51QPCh. 10 - Arrange the following species in order of...Ch. 10 - Prob. 10.53QPCh. 10 - Which of these species has a longer bond, B2 or...Ch. 10 - Acetylene (C2H2) has a tendency to lose two...Ch. 10 - Compare the Lewis and molecular orbital treatments...Ch. 10 - Explain why the bond order of N2 is greater than...Ch. 10 - Compare the relative stability of the following...Ch. 10 - Use molecular orbital theory to compare the...Ch. 10 - A single bond is almost always a sigma bond, and a...Ch. 10 - In 2009 the ion N23 was isolated. Use a molecular...Ch. 10 - The following potential energy curve represents...Ch. 10 - Prob. 10.63QPCh. 10 - Prob. 10.64QPCh. 10 - Prob. 10.65QPCh. 10 - Explain why the symbol on the left is a better...Ch. 10 - Determine which of these molecules has a more...Ch. 10 - Nitryl fluoride (FNO2) is very reactive...Ch. 10 - Describe the bonding in the nitrate ion NO3 in...Ch. 10 - Prob. 10.70QPCh. 10 - Which of the following species is not likely to...Ch. 10 - Draw the Lewis structure of mercury(II) bromide....Ch. 10 - Sketch the bond moments and resultant dipole...Ch. 10 - Although both carbon and silicon are in Group 4A,...Ch. 10 - Acetaminophen is the active ingredient in Tylenol....Ch. 10 - Caffeine is a stimulant drug present in coffee....Ch. 10 - Predict the geometry of sulfur dichloride (SCl2)...Ch. 10 - Antimony pentafluoride, SbF5, reacts with XeF4 and...Ch. 10 - Draw Lewis structures and give the other...Ch. 10 - Predict the bond angles for the following...Ch. 10 - Briefly compare the VSEPR and hybridization...Ch. 10 - Describe the hybridization state of arsenic in...Ch. 10 - Draw Lewis structures and give the other...Ch. 10 - Which of the following molecules and ions are...Ch. 10 - Prob. 10.85QPCh. 10 - The N2F2 molecule can exist in either of the...Ch. 10 - Cyclopropane (C3H6) has the shape of a triangle in...Ch. 10 - The compound 1,2-dichloroethane (C2H4Cl2) is...Ch. 10 - Does the following molecule have a dipole moment?...Ch. 10 - So-called greenhouse gases, which contribute to...Ch. 10 - The bond angle of SO2 is very close to 120, even...Ch. 10 - 3-azido-3-deoxythymidine, shown here, commonly...Ch. 10 - The following molecules (AX4Y2) all have...Ch. 10 - The compounds carbon tetrachloride (CCl4) and...Ch. 10 - Prob. 10.95QPCh. 10 - What are the hybridization states of the C and N...Ch. 10 - Use molecular orbital theory to explain the...Ch. 10 - Referring to the Chemistry in Action essay...Ch. 10 - Which of the molecules (a)(c) are polar?Ch. 10 - Prob. 10.100QPCh. 10 - The stable allotropic form of phosphorus is P4, in...Ch. 10 - Referring to Table 9.4, explain why the bond...Ch. 10 - Use molecular orbital theory to explain the...Ch. 10 - The ionic character of the bond in a diatomic...Ch. 10 - Prob. 10.105QPCh. 10 - Prob. 10.106QPCh. 10 - Aluminum trichloride (AlCl3) is an...Ch. 10 - The molecules cis-dichloroethylene and...Ch. 10 - Prob. 10.109QPCh. 10 - Prob. 10.110QPCh. 10 - The molecule benzyne (C6H4) is a very reactive...Ch. 10 - Assume that the third-period element phosphorus...Ch. 10 - Consider a N2 molecule in its first excited...Ch. 10 - Prob. 10.114QPCh. 10 - Prob. 10.116QPCh. 10 - Draw the Lewis structure of ketene (C2H2O) and...Ch. 10 - TCDD, or 2,3,7,8-tetrachlorodibenzo-p-dioxin, is a...Ch. 10 - Write the electron configuration of the cyanide...Ch. 10 - Prob. 10.120QPCh. 10 - The geometries discussed in this chapter all lend...Ch. 10 - Prob. 10.122QPCh. 10 - Which of the following ions possess a dipole...Ch. 10 - Given that the order of molecular orbitals for NO...Ch. 10 - Shown here are molecular models of SX4 for X = F,...Ch. 10 - Based on what you have learned from this chapter...Ch. 10 - How many carbon atoms are contained in one square...
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- PROBLEMS Q1) Label the following salts as either acidic, basic, or neutral a) Fe(NOx) c) AlBr b) NH.CH COO d) HCOON (1/2 mark each) e) Fes f) NaBr Q2) What is the pH of a 0.0750 M solution of sulphuric acid?arrow_forward8. Draw all the resonance forms for each of the fling molecules or ions, and indicate the major contributor in each case, or if they are equivalent (45) (2) -PH2 سمة مدarrow_forwardA J то گای ه +0 Also calculate the amount of starting materials chlorobenzaldehyde and p-chloroacetophenone required to prepare 400 mg of the given chalcone product 1, 3-bis(4-chlorophenyl)prop-2-en-1-one molar mass ok 1,3-bis(4-Chlorophenyl) prop-2-en-1-one = 277.1591m01 number of moles= 0.400/277.15 = 0.00144 moles 2 x 0.00 144=0.00288 moves arams of acetophenone = 0.00144 X 120.16 = 0.1739 0.1739x2=0.3469 grams of benzaldehyde = 0.00144X106.12=0.1539 0.1539x2 = 0.3069 Starting materials: 0.3469 Ox acetophenone, 0.3069 of benzaldehyde 3arrow_forward
- 1. Answer the questions about the following reaction: (a) Draw in the arrows that can be used make this reaction occur and draw in the product of substitution in this reaction. Be sure to include any relevant stereochemistry in the product structure. + SK F Br + (b) In which solvent would this reaction proceed the fastest (Circle one) Methanol Acetone (c) Imagine that you are working for a chemical company and it was your job to perform a similar reaction to the one above, with the exception of the S atom in this reaction being replaced by an O atom. During the reaction, you observe the formation of three separate molecules instead of the single molecule obtained above. What is the likeliest other products that are formed? Draw them in the box provided.arrow_forward3. For the reactions below, draw the arrows corresponding to the transformations and draw in the boxes the reactants or products as indicated. Note: Part A should have arrows drawn going from the reactants to the middle structure and the arrows on the middle structure that would yield the final structure. For part B, you will need to draw in the reactant before being able to draw the arrows corresponding to product formation. A. B. Rearrangement ΘΗarrow_forward2. Draw the arrows required to make the following reactions occur. Please ensure your arrows point from exactly where you want to exactly where you want. If it is unclear from where arrows start or where they end, only partial credit will be given. Note: You may need to draw in lone pairs before drawing the arrows. A. B. H-Br 人 C Θ CI H Cl Θ + Br Oarrow_forward
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- Answers to the remaining 6 questions will be hand-drawn on paper and submitted as a single file upload below: Review of this week's reaction: H₂NCN (cyanamide) + CH3NHCH2COOH (sarcosine) + NaCl, NH4OH, H₂O ---> H₂NC(=NH)N(CH3)CH2COOH (creatine) Q7. Draw by hand the reaction of creatine synthesis listed above using line structures without showing the Cs and some of the Hs, but include the lone pairs of electrons wherever they apply. (4 pts) Q8. Considering the Zwitterion form of an amino acid, draw the Zwitterion form of Creatine. (2 pts) Q9. Explain with drawing why the C-N bond shown in creatine structure below can or cannot rotate. (3 pts) NH2(C=NH)-N(CH)CH2COOH This bond Q10. Draw two tautomers of creatine using line structures. (Note: this question is valid because problem Q9 is valid). (4 pts) Q11. Mechanism. After seeing and understanding the mechanism of creatine synthesis, students should be ready to understand the first half of one of the Grignard reactions presented in a past…arrow_forwardPropose a synthesis pathway for the following transformations. b) c) d)arrow_forwardThe rate coefficient of the gas-phase reaction 2 NO2 + O3 → N2O5 + O2 is 2.0x104 mol–1 dm3 s–1 at 300 K. Indicate whether the order of the reaction is 0, 1, or 2.arrow_forward
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