General, Organic, and Biological Chemistry (3rd Edition)
3rd Edition
ISBN: 9780134042428
Author: Laura D. Frost, S. Todd Deal
Publisher: PEARSON
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Chapter 4, Problem 4.14PP
Write the condensed structure for the straight-chain
- a. propane
- b. decane
- c. nonane
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Chapter 4 Solutions
General, Organic, and Biological Chemistry (3rd Edition)
Ch. 4 - Prob. 4.1PPCh. 4 - Prob. 4.2PPCh. 4 - Prob. 4.3PPCh. 4 - Draw a skeletal structure for ethane, C2H6. Do you...Ch. 4 - Prob. 4.5PPCh. 4 - Prob. 4.6PPCh. 4 - Draw a Lewis structure for each of the following...Ch. 4 - Draw a Lewis structure for each of the following...Ch. 4 - Prob. 4.9PPCh. 4 - Prob. 4.10PP
Ch. 4 - Prob. 4.11PPCh. 4 - Prob. 4.12PPCh. 4 - Write the condensed structure for the...Ch. 4 - Write the condensed structure for the...Ch. 4 - Write the skeletal structure for the alkane shown:...Ch. 4 - Write the skeletal structure for the alkane shown:...Ch. 4 - Identify the family of hydrocarbon present in the...Ch. 4 - Identify the family of hydrocarbon present in the...Ch. 4 - Identify all the functional groups present in the...Ch. 4 - Prob. 4.20PPCh. 4 - The most prevalent fatty acid in coconut oil is...Ch. 4 - The most common fatty acid found in animals is...Ch. 4 - Draw the condensed structural formula for each of...Ch. 4 - Give the correct name for each of the following...Ch. 4 - Draw the skeletal structure for each of the...Ch. 4 - Prob. 4.26PPCh. 4 - Prob. 4.27PPCh. 4 - Prob. 4.28PPCh. 4 - Prob. 4.29PPCh. 4 - Prob. 4.30PPCh. 4 - Determine the relationship between each of the...Ch. 4 - Determine the relationship between each of the...Ch. 4 - Determine if each of the following cycloalkanes or...Ch. 4 - Determine it each of the following cycloalkanes or...Ch. 4 - Mark the chiral centers in the following...Ch. 4 - Mark the chiral centers in the following...Ch. 4 - Convert each of the Lewis structures shown into a...Ch. 4 - Convert each of the Lewis structures in Problem...Ch. 4 - Prob. 4.39APCh. 4 - Prob. 4.40APCh. 4 - Convert the skeletal structures shown to condensed...Ch. 4 - Convert the skeletal structures shown to condensed...Ch. 4 - Prob. 4.43APCh. 4 - Prob. 4.44APCh. 4 - Alkanes are also referred to as saturated...Ch. 4 - Are alkanes considered polar or nonpolar...Ch. 4 - Give the skeletal structure and name of the...Ch. 4 - Give the skeletal structure and name of the...Ch. 4 - Name the following straight-chain alkanes or...Ch. 4 - Name the following straight-chain alkanes or...Ch. 4 - Explain the structural difference between a...Ch. 4 - Prob. 4.52APCh. 4 - Identify all of the functional groups in each of...Ch. 4 - Identify all of the functional groups in each of...Ch. 4 - Prob. 4.55APCh. 4 - Prob. 4.56APCh. 4 - Prob. 4.57APCh. 4 - Draw skeletal structures for each of the following...Ch. 4 - Prob. 4.59APCh. 4 - Prob. 4.60APCh. 4 - Prob. 4.61APCh. 4 - Prob. 4.62APCh. 4 - Prob. 4.63APCh. 4 - Prob. 4.64APCh. 4 - Prob. 4.65APCh. 4 - Prob. 4.66APCh. 4 - How many structural isomers are possible for the...Ch. 4 - Prob. 4.68APCh. 4 - Prob. 4.69APCh. 4 - Prob. 4.70APCh. 4 - For each of the following compounds, indicate...Ch. 4 - Prob. 4.72APCh. 4 - Determine whether each of the following is the cis...Ch. 4 - Determine whether each of the following is the cis...Ch. 4 - Prob. 4.75APCh. 4 - Prob. 4.76APCh. 4 - Mark the chiral centers in the following...Ch. 4 - Mark the chiral centers in the following...Ch. 4 - Prob. 4.79APCh. 4 - Prob. 4.80APCh. 4 - Prob. 4.81CPCh. 4 - Prob. 4.82CPCh. 4 - Prob. 1IA.1QCh. 4 - Prob. 1IA.2QCh. 4 - Prob. 1IA.3QCh. 4 - Prob. 1IA.4QCh. 4 - Prob. 1IA.5QCh. 4 - Prob. 1IA.6QCh. 4 - Prob. 1IA.7QCh. 4 - Prob. 1IA.8QCh. 4 - Prob. 1IA.9QCh. 4 - Prob. 1IA.10QCh. 4 - Prob. 1IA.11QCh. 4 - Prob. 2IA.1QCh. 4 - Prob. 2IA.2QCh. 4 - Prob. 2IA.3QCh. 4 - Prob. 2IA.4QCh. 4 - Prob. 2IA.5QCh. 4 - What is the molecular shape (geometry) of the...Ch. 4 - Prob. 2IA.7QCh. 4 - Prob. 1ICCh. 4 - Prob. 2ICCh. 4 - Prob. 3ICCh. 4 - Prob. 4IC
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- When 15.00 mL of 3.00 M NaOH was mixed in a calorimeter with 12.80 mL of 3.00 M HCl, both initially at room temperature (22.00 C), the temperature increased to 29.30 C. The resultant salt solution had a mass of 27.80 g and a specific heat capacity of 3.74 J/Kg. What is heat capacity of the calorimeter (in J/C)? Note: The molar enthalpy of neutralization per mole of HCl is -55.84 kJ/mol.arrow_forwardWhen 15.00 mL of 3.00 M NaOH was mixed in a calorimeter with 12.80 mL of 3.00 M HCl, both initially at room temperature (22.00 C), the temperature increased to 29.30 C. The resultant salt solution had a mass of 27.80 g and a specific heat capacity of 3.74 J/Kg. What is heat capacity of the calorimeter (in J/C)? Note: The molar enthalpy of neutralization per mole of HCl is -55.84 kJ/mol. Which experimental number must be initialled by the Lab TA for the first run of Part 1 of the experiment? a) the heat capacity of the calorimeter b) Mass of sample c) Ti d) The molarity of the HCl e) Tfarrow_forwardPredict products for the Following organic rxn/s by writing the structurels of the correct products. Write above the line provided" your answer D2 ①CH3(CH2) 5 CH3 + D₂ (adequate)" + 2 mited) 19 Spark Spark por every item. 4 CH 3 11 3 CH 3 (CH2) 4 C-H + CH3OH CH2 CH3 + CH3 CH2OH 0 CH3 fou + KMnDy→ C43 + 2 KMn Dy→→ C-OH ") 0 C-OH 1110 (4.) 9+3 =C CH3 + HNO 3 0 + Heat> + CH3 C-OH + Heat CH2CH3 - 3 2 + D Heat H 3 CH 3 CH₂ CH₂ C = CH + 2 H₂ → 2 2arrow_forward
- When 15.00 mL of 3.00 M NaOH was mixed in a calorimeter with 12.80 mL of 3.00 M HCl, both initially at room temperature (22.00 C), the temperature increased to 29.30 C. The resultant salt solution had a mass of 27.80 g and a specific heat capacity of 3.74 J/Kg. What is heat capacity of the calorimeter (in J/C)? Note: The molar enthalpy of neutralization per mole of HCl is -55.84 kJ/mol.arrow_forwardQ6: Using acetic acid as the acid, write the balanced chemical equation for the protonation of the two bases shown (on the -NH2). Include curved arrows to show the mechanism. O₂N- O₂N. -NH2 -NH2 a) Which of the two Bronsted bases above is the stronger base? Why? b) Identify the conjugate acids and conjugate bases for the reactants. c) Identify the Lewis acids and bases in the reactions.arrow_forwardQ5: For the two reactions below: a) Use curved electron-pushing arrows to show the mechanism for the reaction in the forward direction. Redraw the compounds to explicitly illustrate all bonds that are broken and all bonds that are formed. b) Label Bronsted acids and bases in the left side of the reactions. c) For reaction A, which anionic species is the weakest base? Which neutral compound is the stronger acid? Is the forward or reverse reaction favored? d) Label Lewis acids and bases, nucleophiles and electrophiles in the left side of the reactions. A. 용 CH3OH я хон CH3O OH B. HBr CH3ONa NaBr CH3OHarrow_forward
- potential energy Br b) Translate the Newman projection below to its wedge-and-dash drawing. F H. OH CH3 CI c) Isopentane (2-methylbutane) is a compound containing a branched carbon chain. Draw a Newman projection of six conformations about the C2-C3 bond of isopentane. On the curve of potential energy versus angle of internal rotation for isopentane, label each energy maximum and minimum with one of the conformations. 0° 。 F A B D C angle of internal rotation E F 360° (=0°) JDownlarrow_forwardQ7: Identify the functional groups in these molecules a) CH 3 b) Aspirin: HO 'N' Capsaicin HO O CH3 CH 3arrow_forwardQ2: Name the following alkanesarrow_forward
- 1. Complete the following table in your laboratory notebook. Substance Formula Methanol CH3OH Ethanol C2H5OH 1-Propanol C3H7OH 1-Butanol C4H9OH Pentane C5H12 Hexane C6H14 Water H₂O Acetone C3H60 Structural Formula Molecular Weight (g/mol) Hydrogen Bond (Yes or No)arrow_forwardQ1: Compare the relative acidity in each pair of compounds. Briefly explain. (a) CH3OH vs NH 3 (b) HF vs CH3COOH (c) NH3 vs CH4 (d) HCI vs HI (e) CH3COOH vs CH3SH (f) H₂C=CH2 vs CH3 CH3 (g) compare the acidity of the two bolded hydrogens O. H N- (h) compare the acidity of the two bolded hydrogens, draw resonance structures to explain H H Harrow_forwardQ3: Rank the following molecules in order of decreasing boiling point: (a) 3-methylheptane; (b) octane; (c) 2,4-dimethylhexane; (d) 2,2,4-trimethylpentane.arrow_forward
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