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Consider the following two molecules: i. O Na OH a. Name each species (i) and (ii)....
Consider the following two molecules: O Nat 2 a. Name each species (i) and (ii). b....
Consider the following two molecules: O Nat 2 a. Name each species (i) and (ii). b. Which of the two species, (i) or (ii), will be more soluble in water? c. Explain your reasoning for (b). (Use clear logic and sentences to explain why one of the compounds (i) or (ii) is more soluble than the other.) HTML Editora BIVA - A - IX EE 3 1. x'x, IEE - Do @ VO T : 12pt - Paragraph - O...
Name Structure 1) ethanol (ethyl alcohol) State (s), (0) H2O Notes CH-CH2-OH Sol., Insol CH4 Sol.,...
Name Structure 1) ethanol (ethyl alcohol) State (s), (0) H2O Notes CH-CH2-OH Sol., Insol CH4 Sol., Insol. IS Is I No change 2) t-butyl alcohol (2-methyl-2- propanol) CH CH3-C-CH3 1 Is Is I No change OH 3) n-hexyl alcohol (1-hexanol) CH3CH,CH,CH,CHCH2-OH 4) dodecanol 5) 1,6-hexanediol CH CH CH CH CHCH OH ОН 6) decanoic acid Part A) save sample for part B OHS Insols decanoic acid Part B) changed to sodium decanoate after rxn with NaOH After adding the NaOH...
six questions plz help i leave rating The missing product from the following reaction is OH...
six questions plz help i leave rating
The missing product from the following reaction is OH NaOH + H20 COH Co Na* H A OrNa* A B C D Question 28 What is the name of the following ether compound? • Previous Which carbon is the alpha, a, carbon? I HO III II IV 11 III IV EXC o Na OH O" Na O Na OH Na Is this monosaccharide a Dor L sugar? CH2OH C=0 H ОН H ОН...
1. For each of the following structures, i. write the IUPAC name. (2 pts.) ii. classify...
1. For each of the following structures, i. write the IUPAC name. (2 pts.) ii. classify each halogen as 1º, 2º, or 3º. (1 pt.) 2. Draw structures for the following alkyl halides. Be sure to indicate any stereochemistry as needed. (2 pts. each) a. 3,6-dibromo-3,6-dichlorononane b. 2-iodo-2-methylpentane Page 3 4. Indicate which alkyl halide you would expect to react more rapidly by an S12 mechanism. (2 pts.) Explain your answer. (2 pts.) 3. i. State which reagent you would...
I. name the following compounds II. write structures for each of the followong structires III.Arrange alkenes from most...
I.
name the following compounds
II. write structures for each of the followong
structires
III.Arrange alkenes from most to least stable
IV. if rearrangement is expected, draw rearranged structure
for wach carbocation
V.
PLEASE HELP, ive been struggling in organic and this is the
review for our 3rd exam. if i can get help (and explanations) for
1-4 it would be a big help
CHM 2210 Examination 3 11/02/18 Directions: Please supply all answers in the spaces provided on both...
Answer all parts. (a) Consider the following molecules C10H22 H.C_04 CH,CHCHCHCH.CH AICI CH206 CH For each...
Answer all parts. (a) Consider the following molecules C10H22 H.C_04 CH,CHCHCHCH.CH AICI CH206 CH For each of the descriptors below, identify one chemical species from the above list. (1) A hydrocarbon. [1 mark] (ii) An organic acid. [1 mark] (iii) A Lewis acid. [1 mark] (iv) A molecule with sp hybridised atoms. [1 mark] (v) A sugar molecule. [1 mark] (vi) A solid waxy compound. [1 mark] (b) Consider the following reaction H CH,OH + CH3CH2COOH (1) Complete the reaction...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the bonding preferences of each atom when you lay out the skeleton of this molecule!) 1. CC Determine the geometry at each "central atom" (a) Does this molecule have any polar bonds? Is the entire molecule polar? (b) What will be the dominant intermolecular force in a sample of this compound? (c) (c) If you had 100.0 g of this compound, how many moles would...
General Chemistry II Part 3. Now let's consider the effect of structure on acid-base properties: There...
General Chemistry II Part 3. Now let's consider the effect of structure on acid-base properties: There are two main factors that determine whether a molecule containing X-H bond will behave as a Bronsted-Lowry acid and donate a proton: the strength of the bond and the polarity of the bond. On one hand, the stronger the X-H bond, the lower the molecule's tendency to donate the proton. On the other hand, the more polar the X-H bond, the higher the molecules...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
2-methylocta-4,6-dien-1-amine Assignment 1: Draw your molecule from IUPAC name
2-methylocta-4,6-dien-1-amineAssignment 1: Draw your molecule from IUPAC
name Using the given IUPAC name, draw your molecule Complete the cover page (p.1) of your portfolio with the
following:o Structural formula of the moleculeo IUPAC name Use a thin, clear binder or report cover to protect the
portfolio Submit the following in the binder:o Cover page as described above (page 1)Assignment 2: Formula, Molar Mass and Functional
Groups On a page titled Expanded Structural Formula draw the expanded
structure of themolecule.o Show...
Consider the following two molecules: O Nat 2 a. Name each species (i) and (ii). b. Which of the two species, (i) or (ii), will be more soluble in water? c. Explain your reasoning for (b). (Use clear logic and sentences to explain why one of the compounds (i) or (ii) is more soluble than the other.) HTML Editora BIVA - A - IX EE 3 1. x'x, IEE - Do @ VO T : 12pt - Paragraph - O...
Name Structure 1) ethanol (ethyl alcohol) State (s), (0) H2O Notes CH-CH2-OH Sol., Insol CH4 Sol., Insol. IS Is I No change 2) t-butyl alcohol (2-methyl-2- propanol) CH CH3-C-CH3 1 Is Is I No change OH 3) n-hexyl alcohol (1-hexanol) CH3CH,CH,CH,CHCH2-OH 4) dodecanol 5) 1,6-hexanediol CH CH CH CH CHCH OH ОН 6) decanoic acid Part A) save sample for part B OHS Insols decanoic acid Part B) changed to sodium decanoate after rxn with NaOH After adding the NaOH...
six questions plz help i leave rating
The missing product from the following reaction is OH NaOH + H20 COH Co Na* H A OrNa* A B C D Question 28 What is the name of the following ether compound? • Previous Which carbon is the alpha, a, carbon? I HO III II IV 11 III IV EXC o Na OH O" Na O Na OH Na Is this monosaccharide a Dor L sugar? CH2OH C=0 H ОН H ОН...
1. For each of the following structures, i. write the IUPAC name. (2 pts.) ii. classify each halogen as 1º, 2º, or 3º. (1 pt.) 2. Draw structures for the following alkyl halides. Be sure to indicate any stereochemistry as needed. (2 pts. each) a. 3,6-dibromo-3,6-dichlorononane b. 2-iodo-2-methylpentane Page 3 4. Indicate which alkyl halide you would expect to react more rapidly by an S12 mechanism. (2 pts.) Explain your answer. (2 pts.) 3. i. State which reagent you would...
I.
name the following compounds
II. write structures for each of the followong
structires
III.Arrange alkenes from most to least stable
IV. if rearrangement is expected, draw rearranged structure
for wach carbocation
V.
PLEASE HELP, ive been struggling in organic and this is the
review for our 3rd exam. if i can get help (and explanations) for
1-4 it would be a big help
CHM 2210 Examination 3 11/02/18 Directions: Please supply all answers in the spaces provided on both...
Answer all parts. (a) Consider the following molecules C10H22 H.C_04 CH,CHCHCHCH.CH AICI CH206 CH For each of the descriptors below, identify one chemical species from the above list. (1) A hydrocarbon. [1 mark] (ii) An organic acid. [1 mark] (iii) A Lewis acid. [1 mark] (iv) A molecule with sp hybridised atoms. [1 mark] (v) A sugar molecule. [1 mark] (vi) A solid waxy compound. [1 mark] (b) Consider the following reaction H CH,OH + CH3CH2COOH (1) Complete the reaction...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the bonding preferences of each atom when you lay out the skeleton of this molecule!) 1. CC Determine the geometry at each "central atom" (a) Does this molecule have any polar bonds? Is the entire molecule polar? (b) What will be the dominant intermolecular force in a sample of this compound? (c) (c) If you had 100.0 g of this compound, how many moles would...
General Chemistry II Part 3. Now let's consider the effect of structure on acid-base properties: There are two main factors that determine whether a molecule containing X-H bond will behave as a Bronsted-Lowry acid and donate a proton: the strength of the bond and the polarity of the bond. On one hand, the stronger the X-H bond, the lower the molecule's tendency to donate the proton. On the other hand, the more polar the X-H bond, the higher the molecules...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
2-methylocta-4,6-dien-1-amineAssignment 1: Draw your molecule from IUPAC
name Using the given IUPAC name, draw your molecule Complete the cover page (p.1) of your portfolio with the
following:o Structural formula of the moleculeo IUPAC name Use a thin, clear binder or report cover to protect the
portfolio Submit the following in the binder:o Cover page as described above (page 1)Assignment 2: Formula, Molar Mass and Functional
Groups On a page titled Expanded Structural Formula draw the expanded
structure of themolecule.o Show...
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