(a)
Interpretation:
The statement “
(a)

Answer to Problem 1MCP
The given statement is true.
Explanation of Solution
Alcohols have strong intermolecular hydrogen bonding. The
On the other hand, the polarity of the amine nitrogen is less than the oxygen in alcohol. The nitrogen amine is less electronegative than oxygen in the alcohol. Therefore, the dipole on
(b)
Interpretation:
The statement “
(b)

Answer to Problem 1MCP
The given statement is false because of the presence of strong intermolecular hydrogen bonding in octanoic acid, it has higher boiling point than
Explanation of Solution
Carboxylic acids have strong intermolecular hydrogen bonding with each other and strong dipole-dipole attractions. The presence of polar carboxyl group and intermolecular hydrogen bonding makes these acids have higher boiling points. The presence of dimers increases the strength of the van der Waals dispersion forces, which makes them have high boiling points.
The ability of primary and secondary amines to form
Hence, the statement “
(c)
Interpretation:
The statement “
(c)

Answer to Problem 1MCP
The given statement is true.
Explanation of Solution
Amine with five or fewer carbon atoms is soluble in water.
(d)
Interpretation:
The statement “
(d)

Answer to Problem 1MCP
The given statement is true.
Explanation of Solution
In
(e)
Interpretation:
The line formula of
(e)

Answer to Problem 1MCP
The given line formula of
Explanation of Solution
The given line formula is,
The above line formula represents
(f)
Interpretation:
The statement “
(f)

Answer to Problem 1MCP
The given statement is false because
Explanation of Solution
(g)
Interpretation:
The statement “
(g)

Answer to Problem 1MCP
The given statement is false because it secondary amine.
Explanation of Solution
The structure of
From the structure of
(h)
Interpretation:
The statement “
(h)

Answer to Problem 1MCP
The given statement is true.
Explanation of Solution
Reduction of amides in the presence of
(i)
Interpretation:
The statement “
(i)

Answer to Problem 1MCP
The given statement is false because they have different structural and molecular formulas.
Explanation of Solution
The structure of
The structure of
(j)
Interpretation:
The statement “The reaction of
(j)

Answer to Problem 1MCP
The given statement is false because the neutralization reaction of the
Explanation of Solution
Hence the given statement is false because the neutralization reaction of
(k)
Interpretation:
The statement “The alkyl ammonium salt would be more water soluble than the amine” has to be predicted as true or false. If the statement is false, the reason for the false statement has to be described.
(k)

Answer to Problem 1MCP
The given statement is true.
Explanation of Solution
By adding a strong acid to a water-insoluble amine, a water-soluble alkylammonium salt can be formed. The salt could be converted back to an amine by reaction with strong base.
Alkyl ammonium salts can neutralize hydroxide ions. Water is formed and the protonated amine cation is converted into an amine. The nitrogen atom of an ammonium salt has a positive charge, alkyl ammonium salts are more water-soluble than amines.
(l)
Interpretation:
The statement “
(l)

Answer to Problem 1MCP
The given statement is false because it is not a cyclic compound.
Explanation of Solution
The structure of
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Chapter 15 Solutions
GENERAL ORG+BIOCHEMISTRY CONNECT ONLY
- 6. For each of the following, fill in the synthesis arrows with reagents and show the intermediates. You DO NOT need to use the same number of arrows that are shown (you may use more or less), but the product must be formed from the reactant. Then write the mechanism of one step in the synthesis (you can choose which step to write the mechanism for), including all reagents required, clearly labeling the nucleophile and electrophile for each step, and using curved arrows to show the steps in the mechanism. a. b. OHarrow_forwardDraw the productsarrow_forwardDraw the correct productsarrow_forward
- E Organic Chemistry Maxwell Draw the correct products, in either order, for the ozonolysis reaction: 1) O3, CH2Cl2, -78 °C Product 1 + Product 2 2) Zn, HOAc Draw product 1. Select Draw Templates More C H O presented by M Draw product 2. Erase Select Draw Templates M / # # carrow_forward✓ edict the products of this organic reaction: ---- ။ A CH3–C−NH–CH2–C−CH3 + KOH ? Specifically, in the drawing area below draw the condensed structure of the product, or products, of this reaction. If there's more than one product, draw them in any arrangement you like, so long as they aren't touching. If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. Explanation Check Click anywhere to draw the first atom of your structure. C 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibiliarrow_forwardPredict the product of this organic reaction: A HO-C-CH3 + CH3NH2 P+ H2O Specifically, in the drawing area below draw the condensed structure of P. If there is no reasonable possibility for P, check the No answer box under the drawing area. Explanation Check Click anywhere to draw the first atom of your structure. marrow_forward
- H 1) OsO4, pyridine 2) Na2SO3 or NaHSO3 in H₂O 2 productsarrow_forward● Biological Macromolecules Naming and drawing cyclic monosaccharides Your answer is incorrect. • Row 1: Your answer is incorrect. Row 3: Your answer is incorrect. • Row 4: Your answer is incorrect. Try again... 0/5 Give the complete common name, including anomer and stereochemistry labels, of the following molecules. You will find helpful information in the ALEKS resource. CH2OH OH OH H H I H OH OH H] H CH2OH H OH ẞ-L-sorbose HOCH2 OH OH H HOCH2 H OH OH H OH H H CH2OH OH H H OH H I- H OH H OH Explanation Recheck W E R % 25 α B Y X & 5 D F G H McGraw Hill LLC. All Rights Reserved. Terms of Use | Pr Parrow_forwardWhat is the missing reactant in this organic reaction? + R -A HO IN + H₂O Specifically, in the drawing area below draw the skeletal ("line") structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer box under the drawing area. Note for advanced students: you may assume no products other than those shown above are formed. Explanation Check Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward
- Stuc X ctclix ALE X A ALE אן A ALEX Lab (195 X Nut x M Inb x NU X NUT X Unt x + → C www-awu.aleks.com/alekscgi/x/Isl.exe/10_u-lgNslkr7j8P3jH-IQ1g8NUi-mObKa_ZLx2twjEhK7mVG6PulJI006NcKTV37JxMpZuyrVCdQolLAKqp_7U3r1GUD3... New Chrome available: Naomi Question 26 of 39 (4 points) | Question Attempt: 1 of Unlimited Give the IUPAC name. 2,3-dimethylhexane Part: 1/2 Part 2 of 2 Draw the skeletal structure of a constitutional isomer of the alkane above that contains a different number of carbons in its longest chain. Skip Part Check Click and drag to start drawing a structure. 3 Finance headline Q Search mwa Harvard Intensifi... X Save For Later 00 dlo HB Submit Assignment 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility a 9:11 PM 4/22/2025arrow_forwardPredict the product of this organic reaction: + NH2 HO A P+ H2O Specifically, in the drawing area below draw the skeletal ("line") structure of P. If there is no reasonable possibility for P, check the No answer box under the drawing area. Click and drag to start drawing a structure. ✓arrow_forward个 Stuc X ctclix ALE X A ALE × A ALE X Lab x (195 × Nut x M Inbx EF 目 → C www-awu.aleks.com/alekscgi/x/Isl.exe/10_u-IgNslkr7j8P3jH-IQ1g8NUi-mObKa_ZLx2twjEhK7mVG6PulJI006NcKTV37JxMpz Chapter 12 HW = Question 27 of 39 (5 points) | Question Attempt: 1 of Unlimited Part: 1/2 Part 2 of 2 Give the IUPAC name. Check 3 50°F Clear ©2025 McGraw Hill L Q Search webp a عالياكarrow_forward
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