(a)
Interpretation:
The structure of amide formed by the reaction of propylamine
Concept Introduction:

Answer to Problem 60P
The propanoic acid
Explanation of Solution
The reaction of carboxylic acid with ammonia or amines forms amide molecules. It involves the formation of water molecule. In this reaction the amine nitrogen atom react with carbonyl carbon atom of carboxylic acid to form amide.
In the reaction of
(b)
Interpretation:
The structure of amide formed by the reaction of
Concept Introduction:
Functional groups are the groups of atoms or atoms which are bonded with parent carbon chain in the organic molecule and are responsible for the physical and chemical properties of the compound. In organic chemistry, there are different functional groups such as carboxylic acid, alcohol, ester, or amide.
Amines are the organic compounds with general chemical formula of R-NH2 or R-NH-R whereas carboxylic acids are the organic molecules with R-COOH as general chemical formula.

Answer to Problem 60P
The Dodecanoic acid
Explanation of Solution
The reaction of carboxylic acid with ammonia or amines forms amide molecules. It involves the formation of water molecule. In this reaction the amine nitrogen atom react with carbonyl carbon atom of carboxylic acid to form amide.
In the reaction of
(c)
Interpretation:
The structure of amide formed by the reaction of
Concept Introduction:
Functional groups are the groups of atoms or atoms which are bonded with parent carbon chain in the organic molecule and are responsible for the physical and chemical properties of the compound. In organic chemistry, there are different functional groups such as carboxylic acid, alcohol, ester, or amide.
Amines are the organic compounds with general chemical formula of R-NH2 or R-NH-R whereas carboxylic acids are the organic molecules with R-COOH as general chemical formula.

Answer to Problem 60P
The formic acid
Explanation of Solution
The reaction of carboxylic acid with ammonia or amines forms amide molecules. It involves the formation of water molecule. In this reaction the amine nitrogen atom react with carbonyl carbon atom of carboxylic acid to form amide.
In the reaction of
(d)
Interpretation:
The structure of amide formed by the reaction of p-methoxybenzoic acid with
Concept Introduction:
Functional groups are the groups of atoms or atoms which are bonded with parent carbon chain in the organic molecule and are responsible for the physical and chemical properties of the compound. In organic chemistry, there are different functional groups such as carboxylic acid, alcohol, ester, or amide.
Amines are the organic compounds with general chemical formula of R-NH2 or R-NH-R whereas carboxylic acids are the organic molecules with R-COOH as general chemical formula.

Answer to Problem 60P
The p-methoxybenzoic acid reacts with
Explanation of Solution
The reaction of carboxylic acid with ammonia or amines forms amide molecules. It involves the formation of water molecule. In this reaction the amine nitrogen atom react with carbonyl carbon atom of carboxylic acid to form amide.
In the reaction of
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Chapter 17 Solutions
CONNECT IA GENERAL ORGANIC&BIO CHEMISTRY
- 4. For the reactions below, draw the expected product. Be sure to indicate relevant stereochemistry or formal charges in the product structure. a) CI, H e b) H lux ligh Br 'Harrow_forwardArrange the solutions in order of increasing acidity. (Note that K (HF) = 6.8 x 10 and K (NH3) = 1.8 × 10-5) Rank solutions from least acidity to greatest acidity. To rank items as equivalent, overlap them. ▸ View Available Hint(s) Least acidity NH&F NaBr NaOH NH,Br NaCIO Reset Greatest acidityarrow_forward1. Consider the following molecular-level diagrams of a titration. O-HA molecule -Aion °° о ° (a) о (b) (c) (d) a. Which diagram best illustrates the microscopic representation for the EQUIVALENCE POINT in a titration of a weak acid (HA) with sodium. hydroxide? (e)arrow_forward
- Answers to the remaining 6 questions will be hand-drawn on paper and submitted as a single file upload below: Review 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) NH2(C=NH)-N(CH)CH2COOH This bond Q10. Draw two tautomers of creatine using line structures. (Note: this question is valid because problem Q9 is valid). (4 pts) Q11. Mechanism. After seeing and understanding the mechanism of creatine synthesis, students should be ready to understand the first half of one of the Grignard reactions presented in a past…arrow_forwardPropose a synthesis pathway for the following transformations. b) c) d)arrow_forwardThe rate coefficient of the gas-phase reaction 2 NO2 + O3 → N2O5 + O2 is 2.0x104 mol–1 dm3 s–1 at 300 K. Indicate whether the order of the reaction is 0, 1, or 2.arrow_forward
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- In the drawing area below, draw the major products of this organic reaction: 1. NaOH ? 2. CH3Br If there are no major products, because nothing much will happen to the reactant under these reaction conditions, check the box under the drawing area instead. No reaction. Click and drag to start drawing a structure. ☐ : A คarrow_forwardPredict the major products of the following organic reaction: NC Δ ? Some important Notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to draw bonds carefully to show important geometric relationships between substituents. Note: if your answer contains a complicated ring structure, you must use one of the molecular fragment stamps (available in the menu at right) to enter the ring structure. You can add any substituents using the pencil tool in the usual way. Click and drag to start drawing a structure. Х аarrow_forwardPredict the major products of this organic reaction. Be sure you use dash and wedge bonds to show stereochemistry where it's important. + ☑ OH 1. TsCl, py .... 文 P 2. t-BuO K Click and drag to start drawing a structure.arrow_forward
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