Homework Answers
Hofmann elimination is the process of creating tertiary amines
and alkenes from the treatment of quaternary ammonium with excess
methyl iodide, and the treatment of the resulting compound with
silver oxide, water, and heat.
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provide the 6 products that can occur after 2 sequential
hofmann eliminations of c7h12 and n(ch3)3....
starting with (2R, 3R)-2-hydroxy-3-methypentane, 1) Provide the reagents that can be used to form the Hofmann...
starting with (2R, 3R)-2-hydroxy-3-methypentane, 1) Provide the reagents that can be used to form the Hofmann product, 2) provide three agents that can be used to form the Zaitsev product, 3) provide the name of your Zaitsev product, and 4) provide a line bond structure of your Zaitsev profuct.
Starting with (2R,3R)-2-hydroxy-3-methylpentane, please 1) provide the reagents that can be used to form the Hofmann...
Starting with (2R,3R)-2-hydroxy-3-methylpentane, please 1) provide the reagents that can be used to form the Hofmann product, 2) provide the reagents that can be used to form the Zaitsev product, 3) provide the name of your Zaitsev product, and 4) provide a line-bond structure of your Zaitsev product.
Starting with (2R,3R)-2-hydroxy-3-methylpentane, please 1) provide the reagents that can be used to form the Hofmann...
Starting with (2R,3R)-2-hydroxy-3-methylpentane, please 1) provide the reagents that can be used to form the Hofmann product, 2) provide the reagents that can be used to form the Zaitsev product, 3) provide the name of your Zaitsev product, and 4) provide a line-bond structure of your Zaitsev product.
Starting with (2R,3R)-2-hydroxy-3-methylpentane, please 1) provide the reagents that can be used to form the Hofmann...
Starting with (2R,3R)-2-hydroxy-3-methylpentane, please 1) provide the reagents that can be used to form the Hofmann product, 2) provide the reagents that can be used to form the Zaitsev product, 3) provide the name of your Zaitsev product, and 4) provide a line-bond structure of your Zaitsev product.
Starting with (2R,3R)-2-hydroxy-3-methylpentane, please 1) provide the reagents that can be used to form the Hofmann...
Starting with (2R,3R)-2-hydroxy-3-methylpentane, please 1) provide the reagents that can be used to form the Hofmann product, 2) provide the reagents that can be used to form the Zaitsev product, 3) provide the name of your Zaitsev product, and 4) provide a line-bond structure of your Zaitsev product.
How to draw products of reaction (Skill builder) Type 1 Type 2 Type 3 1) Using...
How to draw products of reaction (Skill builder) Type 1 Type 2 Type 3 1) Using the scheme, determine what is your intermediate. It depends on reactants 2) Type 1: Markovnikoy, no preference for sin and anti- draw two products with wedges and dashes; check rearrangement BH TO Type 2- anti addition only, no need in HOR Markovnikov rule, no rearrangement Type 3-sin addition only, anti-Markovnikow no rearrangement CC formation-Zaltsev rule 3) After you draw products: check if product can...
1. Please provide the major products of Friday's reaction: n-Bu NBP NaOH, H2O снэ CH3 2....
1. Please provide the major products of Friday's reaction: n-Bu NBP NaOH, H2O снэ CH3 2. Please provide an arrow-pushing mechanism for the above reaction - Williamson ether synthesis. (You do not have to account for the n-Bu-NBr in the mechanism)
3. Give the products for the following reactions (6 points). Нас он more HCI Hello a....
3. Give the products for the following reactions (6 points). Нас он more HCI Hello a. o n 1. NaH on 2. CH CH CH(CH3)CH2CI ou CHICAS CHICA (LOH SOCI pyridine LOH HBr d. tor HBT
H 3. a) Showing arrow-pushing, draw the products of these acid-base reactions. [10 pts Нас H-N...
H 3. a) Showing arrow-pushing, draw the products of these acid-base reactions. [10 pts Нас H-N H b) From your knowledge of pKa values, predict whether the reactions in part (a) are favorable or not by circling an option below: [4 pts) K<1 reaction () K>1 K 1 K 1 K<1 K>1 reaction (i) 4. A chemist wishes to completely convert the acid shown in the equation below to its conjugate base. Complete the acid-base reaction by selecting one of...
Write the products of these reactions -NH2 1. NaNO2, HCI 2. CuCN 1. N(CH3)3 2. Ag20,...
Write the products of these reactions
-NH2 1. NaNO2, HCI 2. CuCN 1. N(CH3)3 2. Ag20, H20 3.A 1. LAIHA 2. H20 NaN3 1. LATHA 2. H2O NaCN 1. LIAH 2. H20 Br NaCN H. Ni HNO3 H2SO4 NaOH H20 1. NaNO2 HCI 2. HBF 4 CH3 HNO3 Na Cr207 H2SO4 H2SO4 Sn HCI 1. NaNO2 HCI 2. CuCN
How to draw products of reaction (Skill builder) Type 1 Type 2 Type 3 1) Using the scheme, determine what is your intermediate. It depends on reactants 2) Type 1: Markovnikoy, no preference for sin and anti- draw two products with wedges and dashes; check rearrangement BH TO Type 2- anti addition only, no need in HOR Markovnikov rule, no rearrangement Type 3-sin addition only, anti-Markovnikow no rearrangement CC formation-Zaltsev rule 3) After you draw products: check if product can...
1. Please provide the major products of Friday's reaction: n-Bu NBP NaOH, H2O снэ CH3 2. Please provide an arrow-pushing mechanism for the above reaction - Williamson ether synthesis. (You do not have to account for the n-Bu-NBr in the mechanism)
3. Give the products for the following reactions (6 points). Нас он more HCI Hello a. o n 1. NaH on 2. CH CH CH(CH3)CH2CI ou CHICAS CHICA (LOH SOCI pyridine LOH HBr d. tor HBT
H 3. a) Showing arrow-pushing, draw the products of these acid-base reactions. [10 pts Нас H-N H b) From your knowledge of pKa values, predict whether the reactions in part (a) are favorable or not by circling an option below: [4 pts) K<1 reaction () K>1 K 1 K 1 K<1 K>1 reaction (i) 4. A chemist wishes to completely convert the acid shown in the equation below to its conjugate base. Complete the acid-base reaction by selecting one of...
Write the products of these reactions
-NH2 1. NaNO2, HCI 2. CuCN 1. N(CH3)3 2. Ag20, H20 3.A 1. LAIHA 2. H20 NaN3 1. LATHA 2. H2O NaCN 1. LIAH 2. H20 Br NaCN H. Ni HNO3 H2SO4 NaOH H20 1. NaNO2 HCI 2. HBF 4 CH3 HNO3 Na Cr207 H2SO4 H2SO4 Sn HCI 1. NaNO2 HCI 2. CuCN
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