General Chemistry: Atoms First
2nd Edition
ISBN: 9780321809261
Author: John E. McMurry, Robert C. Fay
Publisher: Prentice Hall
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Textbook Question
Chapter 4.4, Problem 4.4P
Use the electronegativity values in Figure 4.4 to predict whether the bonds in the following compounds are polar covalent or ionic:
- (a) SiCl4
- (b) CsBr
- (c) FeBr3
- (d) CH4
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Predict the major products of this organic reaction:
HBr (1 equiv)
cold
?
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.
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Explanation
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Q14. Fill this chart: (please refer to ppt notes/browser to answer these questions)
What alcohol is also called wood alcohol?
What is the common name of ethanol?
Draw the structure of phenol and thiophene?
Are bigger chain alcohol like heptanol and octanol
are soluble or insoluble in water and explain it ?
Are ethers soluble or insoluble in water?
What suffix and prefix are used for alcohol while
naming alcohol and ether?
What the process called when we add water to any
alkene to make alcohol?
Q16. Draw the diagram of following aromatic compound (practice from previous module)
Aniline
Phenol
Benzoic acid
Methyl benzoate
Q17. a. Write the oxidation reactions for the 2 propanol.
b. Write the oxidation reaction of the ethanol.
Question 11 of 18 (1 point) Question Attempt: 3 of
How many signals do you expect in the 'H NMR spectrum for this molecule?
Br
Br
Write the answer below.
Also, in each of the drawing areas below is a copy of the molecule, with Hs shown. In each copy, one of the H atoms is colored red. Highlight in red all other H
atoms that would contribute to the same signal as the H already highlighted red.
Note for advanced students: In this question, any multiplet is counted as one signal.
Number of signals in the 'H NMR spectrum.
1
For the molecule in the top drawing area, highlight in red any other H atoms that will contribute to
the same signal as the H atom already highlighted red.
If no other H atoms will contribute, check the box at right.
No additional Hs to color in top
molecule
Check
For the molecule in the bottom drawing area, highlight in red any other H atoms that will contribute
to the same signal as the H atom already highlighted red.
If no other H atoms will contribute, check the box…
Chapter 4 Solutions
General Chemistry: Atoms First
Ch. 4.2 - Prob. 4.1PCh. 4.2 - Prob. 4.2PCh. 4.2 - Prob. 4.3CPCh. 4.4 - Use the electronegativity values in Figure 4.4 to...Ch. 4.4 - Order the following compounds according to the...Ch. 4.4 - An electrostatic potential map of water is shown...Ch. 4.5 - Prob. 4.7PCh. 4.5 - Write formulas for compounds with the following...Ch. 4.5 - Prob. 4.9CPCh. 4.6 - Draw electron-dot structures for the following...
Ch. 4.6 - Draw an electron-dot structure for the hydronium...Ch. 4.7 - Draw electron-dot structures for the following...Ch. 4.7 - There are two molecules with the formula C2H6O....Ch. 4.7 - The following structure is a representation of...Ch. 4.8 - Carbon monoxide, CO, is a deadly gas produced by...Ch. 4.8 - Draw an electron-dot structure for each of the...Ch. 4.8 - Prob. 4.17PCh. 4.9 - Prob. 4.18PCh. 4.9 - Draw as many resonance structures as possible for...Ch. 4.9 - The following structure shows the connections...Ch. 4.10 - Calculate the formal charge on each atom in the...Ch. 4.10 - Calculate the formal charge on each atom in the...Ch. 4.10 - What is a radical, and why are they so reactive?Ch. 4.10 - Prob. 4.24PCh. 4.10 - Draw an electron-dot structure for the ethyl...Ch. 4 - Two electrostatic potential maps are shown, one of...Ch. 4 - Prob. 4.27CPCh. 4 - Prob. 4.28CPCh. 4 - Prob. 4.29CPCh. 4 - Sinapaldehyde, a compound present in the toasted...Ch. 4 - Vitamin C (ascorbic acid) has the following...Ch. 4 - What general trends in electronegativity occur in...Ch. 4 - Prob. 4.33SPCh. 4 - Prob. 4.34SPCh. 4 - Prob. 4.35SPCh. 4 - Prob. 4.36SPCh. 4 - Prob. 4.37SPCh. 4 - Prob. 4.38SPCh. 4 - Show the direction of polarity for each of the...Ch. 4 - Prob. 4.40SPCh. 4 - Prob. 4.41SPCh. 4 - Prob. 4.42SPCh. 4 - Prob. 4.43SPCh. 4 - Prob. 4.44SPCh. 4 - Prob. 4.45SPCh. 4 - Prob. 4.46SPCh. 4 - Prob. 4.47SPCh. 4 - Prob. 4.48SPCh. 4 - Prob. 4.49SPCh. 4 - Prob. 4.50SPCh. 4 - Which of the following substances contains an atom...Ch. 4 - Draw electron-dot structures for the following...Ch. 4 - Prob. 4.53SPCh. 4 - Oxalic acid, H2C2O4, is a mildly poisonous...Ch. 4 - Draw an electron-dot structure for carbon...Ch. 4 - Prob. 4.56SPCh. 4 - Prob. 4.57SPCh. 4 - Prob. 4.58SPCh. 4 - Prob. 4.59SPCh. 4 - Methylphenidate (C14H19NO2), marketed as Ritalin,...Ch. 4 - Pregabalin (C8H17NO2), marketed as Lyrica, is an...Ch. 4 - Draw as many resonance structures as you can that...Ch. 4 - Prob. 4.63SPCh. 4 - Which of the following pairs of structures...Ch. 4 - Which of the following pairs of structures...Ch. 4 - Draw an electron-dot structure for carbon...Ch. 4 - Prob. 4.67SPCh. 4 - Prob. 4.68SPCh. 4 - Prob. 4.69SPCh. 4 - Prob. 4.70SPCh. 4 - Prob. 4.71SPCh. 4 - Prob. 4.72SPCh. 4 - Prob. 4.73SPCh. 4 - Prob. 4.74CHPCh. 4 - Thiofulminic acid, , is a highly reactive...Ch. 4 - Draw two resonance structures for methyl...Ch. 4 - Prob. 4.78CHPCh. 4 - Prob. 4.79CHPCh. 4 - Prob. 4.80CHPCh. 4 - Prob. 4.81CHPCh. 4 - Prob. 4.82CHPCh. 4 - Prob. 4.83CHPCh. 4 - Prob. 4.84CHPCh. 4 - Prob. 4.85CHPCh. 4 - Sulfur reacts with chlorine to give a product that...Ch. 4 - Sulfur reacts with ammonia to give a product A...Ch. 4 - Prob. 4.88MPCh. 4 - Prob. 4.89MP
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