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10.23 Each compound given in this problem is a common organic solvent. From each pair of...
Part A In the following pair of compounds, select the compound with the higher boiling point....
Part A In the following pair of compounds, select the compound with the higher boiling point. CH-C-CH, O CH:--CH-CH2-OH Submit Request Answer Part B In the following pair of compounds, select the compound with the higher boiling point. CH-CH2-CH-CH: CH-CH-CH
plus state the reason why the following nucleophile is better nucleophile from the reasons given in...
plus state the reason why the following nucleophile is
better nucleophile from the reasons given in pic.
Question 2 16 pts H2S vs. H2O A Pair 1 B VS. в OH Pair 2 VS. CI (protic solvent) OH A vs. H2O Pair 3 B Pair 4 " CH,CH NH2 vs. CH.CH OH Pair 5 B (aprotic solvent) A Pair 6 B NH2 o vs. Pair 7 F vs. M Pair 8 B A B For each of the given pairs...
The following compounds are given: 7. The following compounds are given: CH₃ H3C-C-CH3 CH₂ Cts o...
The following compounds are given:
7. The following compounds are given: CH₃ H3C-C-CH3 CH₂ Cts o n on OH 1. Which compound will have the lowest boiling point? 2. Which compound will have the highest boiling point? 3. Which compound/s will be soluble in C.H14? 4. Which compound/s will be soluble in water? 5. Which compound has the highest intermolecular forces? 6. Rank all 5 compounds from lowest to highest solubility in water
a) CH₂ CH₂ CH2 CH2 WHlyt + ci PRACTICE PROBLEM 18.6 Label each compound as water...
a) CH₂ CH₂ CH2 CH2 WHlyt + ci PRACTICE PROBLEM 18.6 Label each compound as water soluble or water insoluble. a. (CH3CH2)2N C. CH3CH2NH2 Worley Soluble Water soluble H (CH2CH2)2NH]* Br CI- I Coastal Carolina Community College CHM 130 Worksheet / Reactions of Organic Compounds PROBLEM 18.10 Draw the products of each acid-base reaction. a. CH3CH2CH2CH2 --NH2 + HCI b. (CH3)2NH + CH3COOH + H₂O - a. CH CH ₂ CH ₂ CH 2 WH y t + ci PRACTICE...
2 Nered For each pair of compounds (a e), indicate the compound that will be faster...
2 Nered For each pair of compounds (a e), indicate the compound that will be faster in the given reaction. If the reaction rates should be approximately the same, indicate that instead. of 2.50 estion Compound A Compound B a or cho Br in E2 reaction CH) el CHE b. or in E2 reaction c. CI or in S, 2 reaction Br H H H Н. d. or in E2 reaction CH Br CH H H H H Br Br...
3.) For each of the following compounds, draw the major organic product of reaction with HCl...
3.) For each of the following compounds, draw the major organic product of reaction with HCl or NaOH and circle whether the starting materials and products will be more soluble in organic solvent or water Benzoic Acid + HCl: Benzoic Acid + NaOH: OH Benzoic Acid Water/Organic Water Organic Fluorenone HС: Fluorenone + NaOH: Fluorenone Water/Organic Water/Organic Веnzocaine + HCi: Benzocaine + N»OH: H2N Benzocaine Water/Organic Water Organic O=
3.) For each of the following compounds, draw the major organic...
a. For each pair of compounds, tell whether the structural formulas shown represent the same compound,...
a. For each pair of compounds, tell whether the structural formulas shown represent the same compound, different compounds that are constitutional isomers or different compounds that are not constitutional isomers. [4 x 1 mark] (1) and (11) and (111) and (iv) and b. Draw a structural formula for each compound. 1 (3E, 62) 2,9-dimethyl-3,6-decadiene (i) 1,6-Heptadiyne (111) 3-phenyl-1.3-butanediol [1 mark] [1 mark] [1 mark] c. Give TWO chemical tests which are indicated by a change in colour, (write the equation...
1. Methyl ethyl ketone (MEK) is a common organic solvent used in lacquers and varnishes. a....
1. Methyl ethyl ketone (MEK) is a common organic solvent used in lacquers and varnishes. a. Show the mechanism of the reaction. Use curved arrows to show bonds breaking and forming. Use acid (H) or base (OH) as needed. O. O methyl ethyl ketone (MEK) b. If two electrophilic functional groups are present in a compound, this reaction is used to protect the ketone group from reacting with a nucleophile. What reaction conditions would you use to convert Compound B...
Do all work on this paper. 1. The compound below on the left has a much...
Do all work on this paper. 1. The compound below on the left has a much higher melting point than its isomer on the right. Explain. (4 points) Tronohon o llottobu 2. Strong acids always protonate amide oxygens and never protonate amide nitrogens. Provide two reasons that explain this fact (4 points). 3. Draw the complete mechanism of the reaction below and indicate the location of "O in the product. (6 points). CH, + 1 equivalent of KOH in water...
Coastal Carolina Community College CHM 130 Worksheet / Reactions of Organic Compounds PROBLEM 18.10 Draw the...
Coastal Carolina Community College CHM 130 Worksheet / Reactions of Organic Compounds PROBLEM 18.10 Draw the products of each acid-base reaction. a. CH3CH,CH CH2 --NH2 + HCI b. (CH3)2NH + CHCOOH a + H₂O - a.)CH₂ CH₂ CH₂ CH2 H3> toi PRACTICE PROBLEM 18.6 Label each compound as water soluble or water insoluble. a. (CH2CH2)2N C. CH3CH2NH2 Water Soluble
Part A In the following pair of compounds, select the compound with the higher boiling point. CH-C-CH, O CH:--CH-CH2-OH Submit Request Answer Part B In the following pair of compounds, select the compound with the higher boiling point. CH-CH2-CH-CH: CH-CH-CH
plus state the reason why the following nucleophile is
better nucleophile from the reasons given in pic.
Question 2 16 pts H2S vs. H2O A Pair 1 B VS. в OH Pair 2 VS. CI (protic solvent) OH A vs. H2O Pair 3 B Pair 4 " CH,CH NH2 vs. CH.CH OH Pair 5 B (aprotic solvent) A Pair 6 B NH2 o vs. Pair 7 F vs. M Pair 8 B A B For each of the given pairs...
The following compounds are given:
7. The following compounds are given: CH₃ H3C-C-CH3 CH₂ Cts o n on OH 1. Which compound will have the lowest boiling point? 2. Which compound will have the highest boiling point? 3. Which compound/s will be soluble in C.H14? 4. Which compound/s will be soluble in water? 5. Which compound has the highest intermolecular forces? 6. Rank all 5 compounds from lowest to highest solubility in water
a) CH₂ CH₂ CH2 CH2 WHlyt + ci PRACTICE PROBLEM 18.6 Label each compound as water soluble or water insoluble. a. (CH3CH2)2N C. CH3CH2NH2 Worley Soluble Water soluble H (CH2CH2)2NH]* Br CI- I Coastal Carolina Community College CHM 130 Worksheet / Reactions of Organic Compounds PROBLEM 18.10 Draw the products of each acid-base reaction. a. CH3CH2CH2CH2 --NH2 + HCI b. (CH3)2NH + CH3COOH + H₂O - a. CH CH ₂ CH ₂ CH 2 WH y t + ci PRACTICE...
2 Nered For each pair of compounds (a e), indicate the compound that will be faster in the given reaction. If the reaction rates should be approximately the same, indicate that instead. of 2.50 estion Compound A Compound B a or cho Br in E2 reaction CH) el CHE b. or in E2 reaction c. CI or in S, 2 reaction Br H H H Н. d. or in E2 reaction CH Br CH H H H H Br Br...
3.) For each of the following compounds, draw the major organic product of reaction with HCl or NaOH and circle whether the starting materials and products will be more soluble in organic solvent or water Benzoic Acid + HCl: Benzoic Acid + NaOH: OH Benzoic Acid Water/Organic Water Organic Fluorenone HС: Fluorenone + NaOH: Fluorenone Water/Organic Water/Organic Веnzocaine + HCi: Benzocaine + N»OH: H2N Benzocaine Water/Organic Water Organic O=
3.) For each of the following compounds, draw the major organic...
a. For each pair of compounds, tell whether the structural formulas shown represent the same compound, different compounds that are constitutional isomers or different compounds that are not constitutional isomers. [4 x 1 mark] (1) and (11) and (111) and (iv) and b. Draw a structural formula for each compound. 1 (3E, 62) 2,9-dimethyl-3,6-decadiene (i) 1,6-Heptadiyne (111) 3-phenyl-1.3-butanediol [1 mark] [1 mark] [1 mark] c. Give TWO chemical tests which are indicated by a change in colour, (write the equation...
1. Methyl ethyl ketone (MEK) is a common organic solvent used in lacquers and varnishes. a. Show the mechanism of the reaction. Use curved arrows to show bonds breaking and forming. Use acid (H) or base (OH) as needed. O. O methyl ethyl ketone (MEK) b. If two electrophilic functional groups are present in a compound, this reaction is used to protect the ketone group from reacting with a nucleophile. What reaction conditions would you use to convert Compound B...
Do all work on this paper. 1. The compound below on the left has a much higher melting point than its isomer on the right. Explain. (4 points) Tronohon o llottobu 2. Strong acids always protonate amide oxygens and never protonate amide nitrogens. Provide two reasons that explain this fact (4 points). 3. Draw the complete mechanism of the reaction below and indicate the location of "O in the product. (6 points). CH, + 1 equivalent of KOH in water...
Coastal Carolina Community College CHM 130 Worksheet / Reactions of Organic Compounds PROBLEM 18.10 Draw the products of each acid-base reaction. a. CH3CH,CH CH2 --NH2 + HCI b. (CH3)2NH + CHCOOH a + H₂O - a.)CH₂ CH₂ CH₂ CH2 H3> toi PRACTICE PROBLEM 18.6 Label each compound as water soluble or water insoluble. a. (CH2CH2)2N C. CH3CH2NH2 Water Soluble
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