
(a)
Interpretation:
The given alcohol is classified as what type of alcohol has to be identified.
Concept Introduction:
Alcohols are classified as primary, secondary, or tertiary depending upon the number of carbon atoms that is bonded to the carbon atom bearing hydroxyl group.
Primary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to only one other carbon atom.
Secondary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to two other carbon atoms.
Tertiary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to three other carbon atoms.
Primary is denoted as
(b)
Interpretation:
The given alcohol is classified as what type of alcohol has to be identified.
Concept Introduction:
Alcohols are classified as primary, secondary, or tertiary depending upon the number of carbon atoms that is bonded to the carbon atom bearing hydroxyl group.
Primary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to only one other carbon atom.
Secondary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to two other carbon atoms.
Tertiary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to three other carbon atoms.
Primary is denoted as
(c)
Interpretation:
The given alcohol is classified as what type of alcohol has to be identified.
Concept Introduction:
Alcohols are classified as primary, secondary, or tertiary depending upon the number of carbon atoms that is bonded to the carbon atom bearing hydroxyl group.
Primary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to only one other carbon atom.
Secondary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to two other carbon atoms.
Tertiary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to three other carbon atoms.
Primary is denoted as
(d)
Interpretation:
The given alcohol is classified as what type of alcohol has to be identified.
Concept Introduction:
Alcohols are classified as primary, secondary, or tertiary depending upon the number of carbon atoms that is bonded to the carbon atom bearing hydroxyl group.
Primary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to only one other carbon atom.
Secondary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to two other carbon atoms.
Tertiary alcohol is the one in which the carbon atom bearing the hydroxyl group is bonded to three other carbon atoms.
Primary is denoted as

Want to see the full answer?
Check out a sample textbook solution
Chapter 3 Solutions
Organic And Biological Chemistry
- First I wanted to see if you would mind checking my graphs behind me. (They haven't been coming out right)? Second, could you help me explain if the rate of reaction is proportional to iodide and persulfate of each graph. I highlighted my answer and understanding but I'm not sure if I'm on the right track. Thank you in advance.arrow_forwardThe heat of combustion for ethane, C2H6C2H6 , is 47.8 kJ/g. How much heat is produced if 1.65 moles of ethane undergo complete combustion?arrow_forwardReview 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)arrow_forward
- Would the following organic synthesis occur in one step? Add any missing products, required catalysts, inorganic reagents, and other important conditions. Please include a detailed explanation and drawings showing how the reaction may occur in one step.arrow_forwardPlease help me answer a. Please and thank you I advance.arrow_forwardDraw both of the chair flips for both the cis and trans isomers for the following compounds: 1,4-diethylcyclohexane 1-methyl-3-secbutylcyclohexanearrow_forward
- Ppplllleeeaaasssseeee hellppp wiithhh thisss physical chemistryyyyy I talked like this because AI is very annoyingarrow_forwardFor this question, if the product is racemic, input both enantiomers in the same Marvin editor. A) Input the number that corresponds to the reagent which when added to (E)-but-2-ene will result in a racemic product. Input 1 for Cl, in the cold and dark Input 2 for Oy followed by H₂O, Zn Input 3 for D₂ with metal catalyst Input 4 for H₂ with metal catalyst B) Draw the skeletal structure of the major organic product made from the reagent in part A Marvin JS Help Edit drawing C) Draw the skeletal structure of the major organic product formed when (2)-but-2-ene is treated with peroxyacetic acid. Marvin 35 Helparrow_forwardMichael Reactions 19.52 Draw the products from the following Michael addition reactions. 1. H&C CH (a) i 2. H₂O* (b) OEt (c) EtO H₂NEt (d) ΕΙΟ + 1. NaOEt 2. H₂O' H H 1. NaOEt 2. H₂O*arrow_forward
- Rank the labeled protons (Ha-Hd) in order of increasing acidity, starting with the least acidic. НОН НЬ OHd Онсarrow_forwardCan the target compound at right be efficiently synthesized in good yield from the unsubstituted benzene at left? ? starting material target If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area. Be sure you follow the standard ALEKS rules for submitting syntheses. + More... Note for advanced students: you may assume that you are using a large excess of benzene as your starting material. C :0 T Add/Remove step Garrow_forwardThe following equations represent the formation of compound MX. What is the AH for the electron affinity of X (g)? X₂ (g) → 2X (g) M (s) → M (g) M (g) M (g) + e- AH = 60 kJ/mol AH = 22 kJ/mol X (g) + e-X (g) M* (g) +X (g) → MX (s) AH = 118 kJ/mol AH = ? AH = -190 kJ/mol AH = -100 kJ/mol a) -80 kJ b) -30 kJ c) -20 kJ d) 20 kJ e) 156 kJarrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningIntroductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning





