
Concept explainers
(a)
Interpretation: The stereogenic center(s) is to be labeled.
Concept introduction: Stereoisomers are the compounds in which molecular formula of a compound remains same but positions of different atoms or groups are changed to form new compounds. The stereogenic centers are also known as sterocenters. The stereocenters are carbon atoms on which the interchanging of two atoms or groups results in the formation of new stereoisomers.
(b)
Interpretation: Amide(s) that can be reduced to form benzphetamine is to be predicted.
Concept introduction:
(c)
Interpretation: The carbonyl compound and amine that can be used to make benzphetamine by reductive amination are to be stated. The possible methods are to be drawn.
Concept introduction: Amines are the derivatives of ammonia consisting of nitrogen atom with the lone pair of electrons. They are basic compounds. The synthesis of the products relies upon the type of reactants and reagents that are used during the reactions. The energy of a target molecule should be low because it increases the stability of a molecule that results in the formation of molecules with high yield. The reagents perform numerous functions in reactions like proton abstraction, oxidation, reduction, catalysis, and dehydrogenation.
(d)
Interpretation: The products which are formed by Hofmann elimination from benzphetamine are to be drawn. The major product is to be labeled.
Concept introduction: Amines are the derivatives of ammonia consisting of nitrogen atom with the lone pair of electrons. They are basic compounds. Hoffman’s elimination reaction involves the less substituted alkene as a more favourable product, whereas according to Zaitsev rule, more substituted

Trending nowThis is a popular solution!

Chapter 25 Solutions
Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card
- Draw a Haworth projection of a common cyclic form of this monosaccharide CH₂OH HO H HO H H OH CH₂OHarrow_forwardCan you explain how I get these here and show the steps plz?arrow_forwardGive the IUPAC name for this compound Hydrocarbon Condensed Formulas Hint C2H5 CH2CH3 expand that in all the formula Part A: (CH3)2CHCH(C2H5)CH2CH2CH3 Give the IUPAC name for this compound. Part B: CH2=C(C2H5)CH2CH2CH3 Give the IUPAC name for this compound. Part C: (CH3)2C=CHC(C2H5)=CH2 Give the IUPAC name for this compound. Part D: CH3C=CCH(C2H5)2 Give the IUPAC name for this compound. Part E: (CH3)3CC=CCH2CH=C(CH3)2arrow_forward
- Select/ Match the correct letter from the image below for the IUPAC names given below: A B C D 3 E F G H K L Part 1. 4-methylheptane For example.mmmm Answer Letter H _for part 1 Part 2. 2,4-dimethylhexane Part 3. 2,3-dimethylpentane Part 4. 2,2-dimethylhexane Part 5. 2-ethyl-1,1,3,3-tetramethylcyclopentane Part 6. 3-ethyl-2-methylpentanearrow_forwardCan u show the process as to how to get these?arrow_forwardSketch the expected 'H NMR spectra for the following compound. Label all of the H's in the structure and the corresponding signal for the spectra you sketch. Make sure you include the integration value and the splitting pattern for each signal Indicate how many signals you would expect in the 13C NMRarrow_forward
- Use IUPAC naming rules to name the following hydrocarbon compounds: CH2-CH3 | a) CH-CH-CH2-CH-CH-CH3 b) | CH2 CH3 | CH3 CH3 \ / C=C H 1 H CH2-CH3 c) d) CH=C-CH3 e) CH3-CH2-CH2-CH=CH-CH3 f) CH2=CH-CH2-CH=CH-CH3 g) CH3-CH2-C = C-CH2-CH3 h)arrow_forwardQ5 Name the following : a. b. C. d. e.arrow_forward25. Predict the major product of the following reaction. 1 equivalent of each of the starting materials was used. H₂C CH3 CH3 H3C H3C H3C. CH2 + H3C. heat CH3 CH H.C. CH3 H.C H.C CH3 CH CH3 CH3 A B C Earrow_forward
- Find chemical structures based on the below information. a) Chemical formula C6H8O Compound is aromatic plus has two 1H NMR peaks that integrated for 3 each that are singlets (it could have more peaks in the 1H NMR b) Chemical Formula: C6H100 Compounds is conjugated 'H NMR has a signal that integrates for 6 and is a doublet IR spectra has a signal at 1730 cm-1arrow_forwardJaslev Propose a synthesis of the following starting from benzene and any other reagents and chemicals. No mechanisms are required. Indicate the condition for each step plus the major product for each step. More than two steps are required. Step 1 Step 2 مہد Brarrow_forwardPart C: The line formula for another branched alkane is shown below. i. In the IUPAC system what is the root or base name of this compound? ii. How many alkyl substituents are attached to the longest chain? iii. Give the IUPAC name for this compound.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningOrganic 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



