Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
expand_more
expand_more
format_list_bulleted
Question
Chapter 3.2, Problem 6P
Interpretation Introduction
(a)
Interpretation: The primary, secondary or tertiary amine in the given compound is to be classified.
Concept introduction:
In secondary amines, two of the hydrogen atoms of ammonia are replaced by alkyl or aryl group.
In tertiary amines, all hydrogen atoms of ammonia are replaced by alkyl or aryl group.
Interpretation Introduction
(b)
Interpretation: The primary, secondary or tertiary amine in the given compound is to be classified.
Concept introduction: Amines are nitrogen-containing organic compounds. The general formula of amines is
In secondary amines, two of the hydrogen atoms of ammonia are replaced by alkyl or aryl group.
In tertiary amines, all hydrogen atoms of ammonia are replaced by alkyl or aryl group.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
Please correct answer and don't used hand raiting
this is an induced approximation. Can
u draw the mechanism ?
요
H
NaOH
1-1
OH
Please correct answer and don't used hand raiting
Chapter 3 Solutions
Organic Chemistry (6th Edition)
Ch. 3.1 - Prob. 1PCh. 3.2 - (a) Classify the carbon atoms in each compound as...Ch. 3.2 - Problem 3.3 Classify a carbon atom by the number...Ch. 3.2 - Classify each alkyl halide and alcohol as , or...Ch. 3.2 - Prob. 5PCh. 3.2 - Prob. 6PCh. 3.2 - Draw the structure of a compound of molecular...Ch. 3.2 - Prob. 8PCh. 3.2 - Prob. 9PCh. 3.2 - Draw the structure of a compound fitting each...
Ch. 3.4 - Predict which compound in each pair has the higher...Ch. 3.4 - Prob. 17PCh. 3.4 - a Label the hydrophobic and hydrophilic portions...Ch. 3.5 - Prob. 21PCh. 3 - 3.29
Identify the functional groups in the...Ch. 3 - Prob. 32PCh. 3 - 3.31 For each alkane: (a) classify each carbon...Ch. 3 - 3.32 Identify the functional groups in each...Ch. 3 - 3.33 Identify each functional group located in the...Ch. 3 - 3.34 (a)Identify the functional groups in...Ch. 3 - Draw seven constitutional isomers with molecular...Ch. 3 - Prob. 38PCh. 3 - Prob. 39PCh. 3 - Prob. 40PCh. 3 - Intramolecular force of attraction are often...Ch. 3 - 3.40 (a) Draw four compounds with molecular...Ch. 3 - 3.41 Rank the compounds in each group in order of...Ch. 3 - Explain why CH3CH2NHCH3 has higher boiling point...Ch. 3 - Prob. 45PCh. 3 - 3.44 Rank the following compounds in order of...Ch. 3 - Prob. 47PCh. 3 - 3.50 Predict the solubility of each of the...Ch. 3 - Prob. 52PCh. 3 - Prob. 53PCh. 3 - 3.53 THC is the active component in marijuana, and...Ch. 3 - Prob. 55PCh. 3 - Prob. 56PCh. 3 - 3.60 Quinapril (trade name Accupril) is a drug...Ch. 3 - 3.61 Answer each question about oxycodone, a...Ch. 3 - Prob. 65PCh. 3 - Prob. 66PCh. 3 - 3.64 Explain why A is less water soluble than B,...Ch. 3 - 3.65 Recall from section 1.10B that there is...
Knowledge Booster
Similar questions
- Please correct answer and don't used hand raitingarrow_forwardPlease correct answer and don't used hand raitingarrow_forward(a) The following synthesis of the molecule shown in the circle has a major problem. What is this problem? (2 pts) 1) HBr (no peroxides) 2) H- NaNH2 Br 3) NaNH, 4) CH3Br 5) H2, Pd (b) Starting with the molecule shown below and any other materials with two carbons or less, write out an alternate synthesis of the circled molecule. More than one step is needed. Indicate the reagent(s) and the major product in all the steps in your synthesis. (5 pts) 2024 Fall Term (1) Organic Chemistry 1 (Lec) CHEM 22204 02[6386] (Hunter College) (c) Using the same starting material as in part (b) and any other materials win two carpons or less, write out syntheses of the circled molecules shown below. More than one step is needed in each case. Indicate the reagent(s) and the major product in all the steps in your synthesis. You may use reactions and products from your synthesis in part (b). (5 pts)arrow_forward
- alt ons for Free Response Questions FRQ 1: 0/5 To spectrophotometrically determine the mass percent of cobalt in an ore containing cobalt and some inert materials, solutions with known [Co?) are prepared and absorbance of each of the solutions is measured at the wavelength of optimum absorbance. The data are used to create a calibration plot, shown below. 0.90- 0.80- 0.70 0.60 0.50 0.40- 0.30 0.20- 0.10- 0.00- 0.005 0.010 Concentration (M) 0.015 A 0.630 g sample of the ore is completely dissolved in concentrated HNO3(aq). The mixture is diluted with water to a final volume of 50.00 ml. Assume that all the cobalt in the ore sample is converted to Co2+(aq). a. What is the [Co2] in the solution if the absorbance of a sample of the solution is 0.74? 13 ✗ b. Calculate the number of moles of Co2+(aq) in the 50.00 mL solution. 0.008 mols Coarrow_forwardPlease correct answer and don't used hand raitingarrow_forwardCloso-boranes and arachno-boranes are structures that exhibit B-B, B-H-B, and B-H bonds. Correct?arrow_forward
- Indicate why boron hydrides cannot form large linear or planar structures.arrow_forwardNido-boranes are structures with the molecular formula BnHn+4 that exhibit B-B, B-H-B and B-H bonds. Correct?arrow_forward8:07 AM Wed Dec 18 Final Exam 2024 copy Home Insert Draw Page Layout Formulas Data Review AA 田 General A G fx Alexis Cozort ☑ ⚫ 61% A B D E F H K M N P R S T U 3+ 10 125 mM that yielded peak heights of Aa = 9 1-(a)A sample solution was examined under XRF to quantify the analyte Ce³+. Find the response factor F, when standardized concentration of analyte [Ce³+]A = concentration of internal standard S i.e. [In³*]s = 151 mM was spiked with standardized 1600 and As = 3015 respectively? 11 12 (i)Define F, F = Aa As [A] [S] + X 13 (*Define with variables) 4000 14 15 (ii)Calculate F, F = numeral (You will use the F value in part 1-(b) below) As 16 (*Calculate with numerals) 17 18 1-(b)To determine the unknown conc of analyte [Ce³+], a volume of 15 mL of internal standard S having a concentration [In³+]s = 0.264 M 19 20 was added to 45 mL of unknown, and the mixture was diluted to 100 mL in a volumetric flask. XRF analysis yielded a spectrum, Figure-1, where peak heights A and As are…arrow_forward
- All structural types of Boron hydrides exhibit B-B, B-H-B and B-H bonds. Correct?arrow_forwardN-nitrosodimethylamine (NDMA) is a suspected carcinogen that can form via reactions between dimethylamine (DMA) and monochloramine (NH2Cl). The relevant elementary reactions and the corresponding rate constants are as shown below. Reaction Rate constant (M¹s¹) DMA + NH2Cl = DMCA + NH3 k =1.4×10-1, kr = 5.83×10-3 1.28×10-3 DMA + NH2Cl → UDMH UDMH + NH2Cl → NDMA -> 1.11×10-1 If the initial concentrations of DMA and NH2Cl are given, you should be able to predict the concentrations of all species at any given reaction time. Please write down the rate equations for DMA, NH2C1, DMCA, UDMH and NDMA.arrow_forwardYou wish to add enough NaOCl (sodium hypochlorite) to a 150 m³ swimming pool to provide a dose of 5.0 mg/L TOTOCI as Cl2. (a) How much NaOCI (kg) should you add? (Note: the equivalent weight of NaOCl is based on the reaction: NaOCl + 2H + 2 e→CI + Na +H₂O.) (10 pts) (atomic weight: Na 23, O 16, C1 35.5) (b) The pH in the pool after the NaOCl addition is 8.67. To improve disinfection, you want at least 90% of the TOTOCI to be in the form of HOCI (pKa 7.53). Assuming that HOCI/OCI is the only weak acid/base group in solution, what volume (L) of 10 N HCl must be added to achieve the goal? (15 pts) Note that part a) is a bonus question for undergraduate students. If you decide not to work on this part of the question, you many assume TOTOCI = 7×10-5 M for part b).arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning