---### Organic Chemistry Reaction ExercisesComplete the following reactions. Write in stereochemistry where relevant. Write "No RXN" if no reaction will occur.#### 1)**Reactant:** Cyclohexanol**Reagent:** PCC (Pyridinium Chlorochromate)![Cyclohexanol to Cyclohexanone](https://via.placeholder.com/100)**Product:** Cyclohexanone_Explanation: Oxidation of alcohol to ketone using PCC._#### 2)**Reactant:** Cyclohexanone**Reagent:** 1) LAH (Lithium Aluminium Hydride) 2) H₂O![Cyclohexanone to Cyclohexanol](https://via.placeholder.com/100)**Product:** Cyclohexanol_Explanation: Reduction of ketone to alcohol using LAH followed by hydrolysis._#### 3)**Reactant:** 4-hydroxybutanal**Reagent:** PCC![4-Hydroxybutanal to 4-Oxo-butanal](https://via.placeholder.com/100)**Product:** 4-Oxo-butanal_Explanation: Oxidation of primary alcohol to aldehyde using PCC._#### 4)**Reactant:** 3-hydroxy-2-methylpropionic acid**Reagent:** _none_ (Product shown)![3-Hydroxy-2-methylpropionic acid to 3-Oxo-2-methylpropionic acid](https://via.placeholder.com/100)**Product:** 3-Oxo-2-methylpropionic acid_Explanation: The 3-hydroxy-2-methylpropionic acid undergoes oxidation of the hydroxyl group to a keto group._---**Note:** Ensure to balance the equations if required and practice drawing the structures accurately.**Graphs/Diagrams Explanation:** No additional graphs or diagrams being present in this image.---

PCC(Pyridinium chlorochromate) Reagent oxidises Primary alcohol to aldehyde, secondary alcohol to…

Answered: Complete the following reactions. Write…

Complete the following reactions. Write in Stereochemistry where relevant. Write No RXN if no reaction will occur. 1) of PCC ₂ рсс, 2) 1)LAH 2) 4,06 песна 3) 4) i OH

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Related questions

Q: Provide an IUPAC name for the compound below. seque ball & stick labels (Specify (E) or (Z)…

A: Answer :

Q: H3C-O-SiH3 ether, which is similar to dimethyleters, was synthesized. This ether is known to be a…

A: In H3C-O-SiH3, Si is a third-row element it has a lower energetic vacant d orbital which can accept…

Q: R req req 2req Keview Topics] Provide an IUPAC name for the structure shown. gy ball & stick Submit…

A: IUPAC nomenclature provides a set of rules to name an organic compound unambiguously. Each IUPAC…

Q: What is an IUPAC name: н нн 人 CH3CH2 н н O (3Z,5E,7E)-3,5,7-Nonatriene O (2Z,4E,6Z)-2,4,6-Nonatriene…

A: Given a Alkene molecule. We have to named by systematic IUPAC name of this Alkene molecule.

Q: Consider 1,3-cyclopentandiol ОН НО a) Draw a pair of 1,3-cyclopentandiol stereoisomers that have a…

A: The molecules with the same molecular formula but different structures are known as isomers. If the…

Q: 1. Name each compound, showing stereochemistry where relevant (a) Ph Ph (b) CH3(CH2);CN (c) `NHCH,…

A: a) The name of the given compound is Benzoic anhydride. b) The name of the given compound is…

Q: 4. Predict the major organic product(s) of the following reactions. Be sure to clearly identify…

A: Given are organic reactions. a. This is a hydroboration followed by oxidation reaction.b. Step 1 is…

Q: a) b) c) e) 10 HBr CH3CH₂OOCH₂CH3 1. Hg(OAc)2, H₂O 2. NaBH4 1) BH3/THF 2) H₂O2 NaOH (aq) cold Cl₂,…

Q: a) 2) Complete the following: Stereochemistry and b) C) o type type OH EAS - Nitration H₂ Lindlar…

A: According to Bartleby Q&A guidelines we are supposed to answer only first three sub parts of…

Q: Br HI (1 eq.),

Q: Draw the products of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry.…

A: The objective of the question is to find the major product in which alkene reacts with OsO4 in the…

Q: 1. ВНз SOCI2 2. NaOH H2O2

A: When an unsymmetrical reagent is added to an un symmetrical alkene then the negative part of the…

Q: Use the References to access important values if needed for this question. Draw the organic product…

A: The given compound is ethanethiol. Under biological conditions, the thiol is oxidized into the…

Q: Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is…

A: If compound contain all C-C single bond, then add suffix 'ane' to the name of the parent chain If…

Q: Predict the major products of the following organic reaction: id. I Some important Notes: .Draw the…

A: This is an example of Diels-Alder reaction. It is a pericyclic reaction which involves…

Q: Fill in the boxes with the structures that complete the reactions. Use wedges and dashes to indicate…

A: Organic reactions are those in which organic reactant react to form organic products. In the given…

Q: Ca) (b) (c) HO,S CI ? H2SO4 HNO3 C, ? FeCla AICI, H,CO

A: As per our guidelines, I can answer only first three sub-parts of the question because you have…

Q: A b. Observe the following reaction shown below. With aid of a mechanism, justify the…

A: To understand and justify the stereochemistry of the products (B and C) in the reaction shown, let's…

Q: Draw the major organic product(s) of the following reactions including stereochemistry when it is…

A: When an alkyne reacts with H2O/HgSO/H2SO4, a ketone will be formed. The reaction is known as the…

Q: stereochemistry when applicable. Br a) b) c) d) c) Br Br 1) Nal 2) NaCN, acetone 1) NaOC(CH3)3, heat…

Q: c) Draw the product of the following Lewis acid-base reaction. Discuss whether the product will…

A: AlCl3 is an Lewis acid which is able to accept lone pairs of any atom in its vacant d Orbital.

Q: For the following reaction, indicate the major product. Be sure to indicate stereochemistry

Q: Complete the reaction map by matching A-E with the given choices. A E Na (s) acetic acid DA Al₂O3…

Q: Provide the structure of the product(s) with stereochemisty if appropriate. If multiple products…

Q: Draw the structures of organic compounds A and B. Indicate stereochemistry where applicable H2…

A: The terminal hydrogen atom of acetylene molecule is highly acidic in nature. In the presence of base…

Q: 1. Fill in the missing reactant, reagent and products. Indicate stereochemistry if necessary. Unless…

Q: please help with part D, E, F:

Q: Alkenes can be converted to alcohols by hydroboration-oxidation. (a) Draw the structure of the…

A: Hydroboration–oxidation reaction: The hydroboration–oxidation reaction is a stereospecific two-step…

Q: 1. Name this compound, including stereochemistry if relevant: H H HOČCH2 CH,COH

Q: 3. For the following reaction, fill in the box with the predominant product or products. You must…

A: Given : structure of reactant.

Q: C(CH3)3X +H20 C(CH3)3OH where (X-F, Cl, Br, I) give reaction with each of halogen as well determine…

A: An organic problem based on SN1 mechanism, which is to be accomplished.

Q: Br 'PROH CH3 (b) KO'Bu heat Ph (а) BUOH ... Br

A: Reactions involving organic compounds are called organic reactions. Organic reactions can be of…

Q: Draw the product(s) of the following reactions. H3C-CEC-CH3 ● 1. BH3/THF 2. H₂O₂ / aqueous NaOH •…

Q: Draw a structural formula for the substitution product of the reaction shown below. H3C Br Na'…

Q: Provide IUPAC names for the following compounds. You must include stereochemical notations (E, Z R,…

A: The naming of an organic compound can be done with help of rules of international union of pure and…

Q: Draw the product(s) of the following reactions. CH3CH₂-CEC-CH3 • You do not have to consider…

A: The reaction of alkynes with BH3 (borane) and H2O2 (hydrogen peroxide) is called…

Q: The following Wittig reactions may produce a mixture of alkene stereoisomers. Write the products for…

A: Witting reaction is reaction of aldehyde with oxophosphetane, resulting the formation of alkene.

Q: Chemistry 3. Complete the following reaction scheme. Give all product(s) and indicate major or minor…

Q: HNO3, H₂SO4 1) Cl2, AlCl3 2) Pd, H₂ pib

A: Given reactions are electrophilic aromatic substitution reactions. The first and second reagents are…

Q: Compound A, C₂H16 reacts with 1 molar equivalent(s) of hydrogen on catalytic hydrogenation. A…

A: Given,The reaction:

Q: i Claisen condensation between a diethyl ester and an ethyl ester followed by saponification,…

A: A Claisen ester condensation is a reaction that involves the formation of a carbon-carbon bond…

Q: 19. Does the name 2-butene indicate which of the stereoisomers above is being referred to? 20. To…

A: The stereoisomers are chemical compounds which are having the same molecular formula, but the…

Question

---
### Organic Chemistry Reaction Exercises

Complete the following reactions. Write in stereochemistry where relevant. Write "No RXN" if no reaction will occur.

#### 1)
**Reactant:** Cyclohexanol

**Reagent:** PCC (Pyridinium Chlorochromate)

![Cyclohexanol to Cyclohexanone](https://via.placeholder.com/100)

**Product:** Cyclohexanone

_Explanation: Oxidation of alcohol to ketone using PCC._

#### 2)
**Reactant:** Cyclohexanone

**Reagent:**
1) LAH (Lithium Aluminium Hydride)
2) H₂O

![Cyclohexanone to Cyclohexanol](https://via.placeholder.com/100)

**Product:** Cyclohexanol

_Explanation: Reduction of ketone to alcohol using LAH followed by hydrolysis._

#### 3)
**Reactant:** 4-hydroxybutanal

**Reagent:** PCC

![4-Hydroxybutanal to 4-Oxo-butanal](https://via.placeholder.com/100)

**Product:** 4-Oxo-butanal

_Explanation: Oxidation of primary alcohol to aldehyde using PCC._

#### 4)
**Reactant:** 3-hydroxy-2-methylpropionic acid

**Reagent:** _none_ (Product shown)

![3-Hydroxy-2-methylpropionic acid to 3-Oxo-2-methylpropionic acid](https://via.placeholder.com/100)

**Product:** 3-Oxo-2-methylpropionic acid

_Explanation: The 3-hydroxy-2-methylpropionic acid undergoes oxidation of the hydroxyl group to a keto group._

---
**Note:** Ensure to balance the equations if required and practice drawing the structures accurately.

**Graphs/Diagrams Explanation:** No additional graphs or diagrams being present in this image.

---

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

SEE SOLUTION Check out a sample Q&A here

Step 1: Introduction

VIEW

Step 2: Explanation

VIEW

Solution

VIEW

Step by step

Solved in 3 steps with 1 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

please help with part A,B,C,D:
Provide either the IUPAC name or the best structure for the information given. Include appropriate stereochemistry where applicable
d) e) b) c) E₂ d) Es in the products. Include stereochemistry where relevant. CH₂₁ CH₂ 1. BH, 2. H₂O₂ OH 100⁰ CH₂OH NaCN 1.0₂ 2. Zn, H H₂O* H, heat.
44a) Draw the bond-line structure of 1,4-dimethyl-cyclohexa-1,3-diene here: STRUCTURE: b) Circle all the sp²-hybridized carbons in your drawing of the structure. c) In the spaces below, draw two potential products from a chlorination reaction (addition of Cl2) with your first structure Product 1: Product 2:
4
rank leaving group abililty: Cl, MeCO2, Me, NMe2, OH
(66). Subject :- Chemistry
Draw the products of attached reaction, including stereoisomers.
Oo.169. Subject :- Chemistry
Predict the products of each reaction. If the product has stereochemistry, draw the products using dash wedge notation. Draw all stereoisomers formed and indicate if the product is achiral or chiral. Draw a mechanism for each reaction clearly showing how the product stereochemistry is produced. You are not required to draw the final step(s) in the mechanism for reactions involving organometallic intermediates.
2a) (2 ) Provide the reagents or products for the following reactions. Include ALL stereochemistry, where appropriate. i). ii) iii) Z-4-octene CHO 1) MCPBA/DCM 2) H₂O* NaOCH, CH,OH .CO.I heat ol NH₂ OH
Write the IUPAC name of compound, showing stereochemistry where relevant.