Concept explainers
(a)
Interpretation:
The alkyl group other than the parent chain which is attached to the N atom in ethanamine structure is to be determined.
Concept Introduction:
The
(b)
Interpretation:
The alkyl group other than the parent chain which is attached to the N atom in 2-methylpentane-3-amine structure is to be determined.
Concept Introduction:
The amine compounds are functional group can be defined as the compounds which consists a basic nitrogen atom with a lone pair. These compounds can be called as the derivative of ammonia in which hydrogen atoms are replaced by substituent such as alkyl group.
(c)
Interpretation:
The alkyl group other than the parent chain which is attached to the N atom in N-methylbutan-2-amine structure is to be determined.
Concept Introduction:
The amine compounds are functional group can be defined as the compounds which consists a basic nitrogen atom with a lone pair. These compounds can be called as the derivative of ammonia in which hydrogen atoms are replaced by substituent such as alkyl group.
(d)
Interpretation:
The alkyl group other than the parent chain which is attached to the N atom in N,2-dimethylpropan-2-amine structure is to be determined.
Concept Introduction:
The amine compounds are functional group can be defined as the compounds which consists a basic nitrogen atom with a lone pair. These compounds can be called as the derivative of ammonia in which hydrogen atoms are replaced by substituent such as alkyl group.
(e)
Interpretation:
The alkyl group other than the parent chain which is attached to the N atom in N,N-diethylpentane-3-amine structure is to be determined.
Concept Introduction:
The amine compounds are functional group can be defined as the compounds which consists a basic nitrogen atom with a lone pair. These compounds can be called as the derivative of ammonia in which hydrogen atoms are replaced by substituent such as alkyl group.
Want to see the full answer?
Check out a sample textbook solutionChapter NW2 Solutions
Organic Chemistry: A Guided Inquiry
- Q5: 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_forwardpotential 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_forward
- Q2: Name the following alkanesarrow_forward1. 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_forward
- Q3: 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_forwardQ5: Conformations of Alkanes a) Draw a Newman Projection of the compound below about the C2-C3 bond. H3C Cli... H IIIH Br CH3arrow_forwardThe ability of atoms to associate with each other depends ona) the electronic structure and its spatial orientation.b) the electron affinity.c) The other two answers are correct.arrow_forward
- What is the final volume after you reach the final temperature? I put 1.73 but the answer is wrong not sure why The initial volume of gas is 1.60 LL , the initial temperature of the gas is 23.0 °C°C , and the system is in equilibrium with an external pressure of 1.2 bar (given by the sum of a 1 bar atmospheric pressure and a 0.2 bar pressure due to a brick that rests on top of the piston). Then, as you did in Exercise 1, you heat the gas slowly until the temperature reaches 48.2 °Carrow_forwardQ4: Identify the type of Carbon ( methyl, primary, secondary, etc. ) indicated by this arrow.arrow_forwardQ3: Curved Arrows, Lewis Acids & Bases, Nucleophiles and Electrophiles Considering the following reactions: a) Predict the products to complete the reactions. b) Use curved electron-pushing arrows to show the mechanism for the reaction in the forward direction. Redraw some of the compounds to explicitly illustrate all bonds that are broken and all bonds that are formed. c) Label Lewis acids and bases, nucleophiles and electrophiles in the reactions. A. S + AICI 3 B. + H₂Oarrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning