CHEMISTRY-W/MASTERING CHEMISTRY ACCESS
8th Edition
ISBN: 9780135205068
Author: Robinson
Publisher: PEARSON
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Chapter 7, Problem 7.68SP
Identify the correct electron-dot structure for
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Part 2 (0.5 point)
0-
Draw the major organic product with the correct geometry.
10
1:
70000 х
く
1st attempt
Part 1 (0.5 point) Feedback
Please draw all four bonds at chiral centers.
P
See Periodic Table See Hint
Heating an alcohol in the presence of sulfuric or phosphoric acid will cause a dehydration to occur: the removal of the elements of water from a
molecule, forming an alkene. The reaction usually follows an E1 mechanism. The SN1 pathway is suppressed by using a strong acid whose conjugate
base is a poor nucleophile. Further, heating the reaction mixture causes a greater increase in the rate of E1 compared to the rate of S№1.
2nd attempt
0
See Periodic Table
See Hint
Draw the organic intermediate from the first step (no byproducts) and draw curved arrow(s) to show how it reacts.
TH
+11:
1st attempt
Feedback
H
H
H
C
F
F
See Periodic Table
See Hint
This molecule undergoes an E1 mechanism when stirred in methanol.
3rd attempt
CH₂OH
CH₂OH
6148
O
See Periodic Table. See Hint
Draw 3 chemical species including formal charges and lone pairs of electrons. Add the missing curved arrow notation.
H
N
O O SA 3
Br
I
Chapter 7 Solutions
CHEMISTRY-W/MASTERING CHEMISTRY ACCESS
Ch. 7 - Use the electro negativity values in Figure 7.4...Ch. 7 - Conceptual APPLY 7.2 An electrostatic potential...Ch. 7 - The dipole moment of AgCI in the gas phaseis...Ch. 7 - Predict which bond has greater percent ionic...Ch. 7 - Select the correct electron-dot structure for H2S...Ch. 7 - Use the octet rule to predict the molecular...Ch. 7 - Identify the correct electron-dot structure for...Ch. 7 - Draw an electron-dot structure for each of the...Ch. 7 - Select the correct electron-dot structure for...Ch. 7 - Identify the correct electron-dot structure(s) for...
Ch. 7 - Prob. 7.11PCh. 7 - Which oxygen species do you predict to be most...Ch. 7 - Draw an electron-dot structure for the following...Ch. 7 - There are two molecules with the formula C2H6O...Ch. 7 - The following structure is a representation of...Ch. 7 - Draw two possible electron-dot structures for the...Ch. 7 - Called “laughing gas, nitrous oxide (N2O) is...Ch. 7 - Draw as many resonance structures as possible for...Ch. 7 - Prob. 7.19PCh. 7 - Prob. 7.20ACh. 7 - Calculate the formal charge on each atom in the...Ch. 7 - Start with the electron-dot structure for the...Ch. 7 - Calculate formal charges on the C and O atoms in...Ch. 7 - Three resonance structures for anisole (Problem...Ch. 7 - The toxicity of the organophosphate insecticides...Ch. 7 - Prob. 7.26PCh. 7 - Prob. 7.27PCh. 7 - The following structure is a representation of the...Ch. 7 - The electron-dot structure for the nerve a gentsar...Ch. 7 - Draw the new electron-dot structures indicated by...Ch. 7 - The following diagram shows the potential energy...Ch. 7 - The following diagram shows the potential energy...Ch. 7 - Two electrostatic potential maps are shown, one of...Ch. 7 - Prob. 7.34CPCh. 7 - Which of the following drawings is most likely to...Ch. 7 - The following ball-and-stick molecular model is a...Ch. 7 - The following hall-and-stick molecular model is a...Ch. 7 - Sinapaldehyde, a compound present in the toasted...Ch. 7 - Vitamin C (ascorbic acid) has the following...Ch. 7 - Match the following descriptions with the type of...Ch. 7 - Why do two atoms come together to form a covalent...Ch. 7 - Explain the difference in the bond dissociation...Ch. 7 - Explain the difference in the bond dissociation...Ch. 7 - Predict which of the following bonds should be...Ch. 7 - Prob. 7.45SPCh. 7 - What general trends in electro negativity occur in...Ch. 7 - Predict the electro negativity of the undiscovered...Ch. 7 - Order the following elements according to...Ch. 7 - Order the following elements according to...Ch. 7 - Which of the following substances contain bonds...Ch. 7 - Use the electro negativity data in Figure 7.4 to...Ch. 7 - Show the direction of polarity for each of the...Ch. 7 - Show the direction of polarity for each of the...Ch. 7 - Which of the substances...Ch. 7 - Which of the substances...Ch. 7 - Order the following compounds according to the...Ch. 7 - Order the following compounds according to the...Ch. 7 - Prob. 7.58SPCh. 7 - Using only the elements Ca, Cl, and Si, give...Ch. 7 - The dipole moment of BrCl is 0.518 D, and the...Ch. 7 - Prob. 7.61SPCh. 7 - Prob. 7.62SPCh. 7 - Prob. 7.63SPCh. 7 - Why does the octet rule apply primarily to...Ch. 7 - Which of the following substances contains an atom...Ch. 7 - Draw electron-dot structures for the following...Ch. 7 - Draw electron-dot structures for the following...Ch. 7 - Identify the correct electron-dot structure for...Ch. 7 - Draw an electron.dot structure for the hydronium...Ch. 7 - Oxalic acid, H2C2O4 , is a mildly poisonous...Ch. 7 - Draw an electron-dot structure for carbon...Ch. 7 - Prob. 7.72SPCh. 7 - Identify the fourth-row elements, X, that form the...Ch. 7 - Write electron-dot structures for molecules with...Ch. 7 - Write electron-dot structures for molecules with...Ch. 7 - Which compound do you expect to have the stronger...Ch. 7 - Which compound do you expect to have the stronger...Ch. 7 - Draw an electron-dot structure for each of the...Ch. 7 - Prob. 7.79SPCh. 7 - Methylphenidate (C14H19NO2) , marketed as Ritalin,...Ch. 7 - Pregabalin (C8H17NO2) , marketed as Lyric a, is an...Ch. 7 - The following molecular model is that of...Ch. 7 - Ibuprofen C 13 H 18 O 2 marketed under such brand...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Draw as many resonance structures as you can for...Ch. 7 - Which of the following pairs of structures...Ch. 7 - Which of the following pairs of structures...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Benzene has the following structural formula. Use...Ch. 7 - Draw three resonance structures for sulfur...Ch. 7 - Some mothballs used when storing clothes are made...Ch. 7 - Four different structures (a), (b), (c), and (d)...Ch. 7 - Draw an electron-dot structure for carbon...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Calculate formal charges for the C and O atoms in...Ch. 7 - Draw two electron-dot resonance structures that...Ch. 7 - Draw two electron-dot resonance structures that...Ch. 7 - Prob. 7.102SPCh. 7 - Prob. 7.103SPCh. 7 - Boron trifluoride reacts with dimethyl ether to...Ch. 7 - Thiofulminic acid, HCNS, has recently been...Ch. 7 - Draw two rcsonancc strutur for methyl isocyanate,...Ch. 7 - In the cyanatc ion. OCN , carbon is the central...Ch. 7 - Prob. 7.108MPCh. 7 - Prob. 7.109MPCh. 7 - Prob. 7.110MPCh. 7 - The neutral OH molecule has been implicated in...Ch. 7 - Prob. 7.112MPCh. 7 - Prob. 7.113MP
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- Complete the mechanism for the E1 reaction below by following the directions written above each of the five boxes. Be sure to include lone pair electrons and nonzero formal charges. 1st attempt Y 0 + Provide the missing curved arrow notation. 01: See Periodic Table See Hint H C Br Iarrow_forwardPlease help answer number 2. Thanks in advance.arrow_forwardHow do I explain this? Thank you!arrow_forward
- When an unknown amine reacts with an unknown acid chloride, an amide with a molecular mass of 163 g/mol (M* = 163 m/z) is formed. In the infrared spectrum, important absorptions appear at 1661, 750 and 690 cm. The 13C NMR and DEPT spectra are provided. Draw the structure of the product as the resonance contributor lacking any formal charges. 13C NMR DEPT 90 200 160 120 80 40 0 200 160 120 80 40 0 DEPT 135 T 200 160 120 80 40 0 Draw the unknown amide. Select Dow Templates More Fragearrow_forwardIdentify the unknown compound from its IR and proton NMR spectra. C4H6O: 'H NMR: 82.43 (1H, t, J = 2 Hz); 8 3.41 (3H, s); 8 4.10 (2H, d, J = 2 Hz) IR: 2125, 3300 cm¹ The C4H6O compound liberates a gas when treated with C2H5 MgBr. Draw the unknown compound. Select Draw с H Templates Morearrow_forwardPlease help with number 6 I got a negative number could that be right?arrow_forward
- 1,4-Dimethyl-1,3-cyclohexadiene can undergo 1,2- or 1,4-addition with hydrogen halides. (a) 1,2-Addition i. Draw the carbocation intermediate(s) formed during the 1,2-addition of hydrobromic acid to 1,4-dimethyl-1,3-cyclohexadiene. ii. What is the major 1,2-addition product formed during the reaction in (i)? (b) 1,4-Addition i. Draw the carbocation intermediate(s) formed during the 1,4-addition of hydrobromic acid to 1,4-dimethyl-1,3-cyclohexadiene. ii. What is the major 1,4-addition product formed from the reaction in (i)? (c) What is the kinetic product from the reaction of one mole of hydrobromic acid with 1,4-dimethyl-1,3-cyclohexadiene? Explain your reasoning. (d) What is the thermodynamic product from the reaction of one mole of hydrobro-mic acid with 1,4-dimethyl-1,3-cyclohexadiene? Explain your reasoning. (e) What major product will result when 1,4-dimethyl-1,3-cyclohexadiene is treated with one mole of hydrobromic acid at - 78 deg * C ? Explain your reasoning.arrow_forwardGive the product of the bimolecular elimination from each of the isomeric halogenated compounds. Reaction A Reaction B. КОВ CH₂ HotBu +B+ ко HOIBU +Br+ Templates More QQQ Select Cv Templates More Cras QQQ One of these compounds undergoes elimination 50x faster than the other. Which one and why? Reaction A because the conformation needed for elimination places the phenyl groups and to each other Reaction A because the conformation needed for elimination places the phenyl groups gauche to each other. ◇ Reaction B because the conformation needed for elimination places the phenyl groups gach to each other. Reaction B because the conformation needed for elimination places the phenyl groups anti to each other.arrow_forwardFive isomeric alkenes. A through each undergo catalytic hydrogenation to give 2-methylpentane The IR spectra of these five alkenes have the key absorptions (in cm Compound Compound A –912. (§), 994 (5), 1643 (%), 3077 (1) Compound B 833 (3), 1667 (W), 3050 (weak shoulder on C-Habsorption) Compound C Compound D) –714 (5), 1665 (w), 3010 (m) 885 (3), 1650 (m), 3086 (m) 967 (5), no aharption 1600 to 1700, 3040 (m) Compound K Match each compound to the data presented. Compound A Compound B Compound C Compound D Compoundarrow_forward
- 7. The three sets of replicate results below were accumulated for the analysis of the same sample. Pool these data to obtain the most efficient estimate of the mean analyte content and the standard deviation. Lead content/ppm: Set 1 Set 2 Set 3 1. 9.76 9.87 9.85 2. 9.42 9.64 9.91 3. 9.53 9.71 9.42 9.81 9.49arrow_forwardDraw the Zaitsev product famed when 2,3-dimethylpentan-3-of undergoes an El dehydration. CH₂ E1 OH H₁PO₁ Select Draw Templates More QQQ +H₂Oarrow_forwardComplete the clean-pushing mechanism for the given ether synthesia from propanol in concentrated sulfurica140°C by adding any mining aloms, bands, charges, nonbonding electron pairs, and curved arrows. Draw hydrogen bonded to cayan, when applicable. ore 11,0 HPC Step 1: Draw curved arrows Step 2: Complete the intend carved Q2Q 56 QQQ Step 3: Complete the intermediate and add curved Step 4: Modify the structures to draw the QQQ QQQarrow_forward
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