How to prepare the following compound, starting with cyclopentene and any other reagents needed?...
Question:
How to prepare the following compound, starting with {eq}\displaystyle \rm cyclopentene {/eq} and any other reagents needed?
{eq}\displaystyle \rm Cyclopentanol {/eq}.
Hydration Reaction:
The addition of water molecule {eq}\rm (H_2O) {/eq} to a certain molecule having multiple bonds is known as hydration reaction. It occurs by formation of a carbocation as an intermediate.
Answer and Explanation: 1
Become a Study.com member to unlock this answer! Create your account
View this answerWe are told to prepare cyclopentanol from cyclopentene.
- We will do the hydration reaction.
- A carbocation is formed as an intermediate.
- The...
See full answer below.
Ask a question
Our experts can answer your tough homework and study questions.
Ask a question Ask a questionSearch Answers
Learn more about this topic:
Get access to this video and our entire Q&A library
What is Hydration? - Definition, Facts & Benefits
from
Chapter 26 / Lesson 8
65K
Why is it important to drink water? See the definition of hydration, read about the hydration process and benefits of hydration, and learn how to stay hydrated.
Related to this Question
- How to prepare the following compound, starting with cyclopentene and any other reagents needed? Methylcyclopentane.
- How to prepare the following compound, starting with cyclopentene and any other reagents needed? 3-Bromocyclopentene.
- How would you prepare the given compound, starting with cyclopentene and any other reagents needed? Cyclopentylmagnesium chloride
- What reagent(s) could you use to convert cyclopentene to the compound below using the fewest possible steps? More than one step may be necessary.
- Starting from cyclohex-2-enone and any other reagents needed, how would you prepare the given substance? (More than one step may be required.)
- Starting from cyclohex-2-enone and any other reagents needed, how would you prepare the mentioned substance? (More than one step may be required.)
- Show all steps in the following synthesis. You may use any other needed reagents but you should begin with the compound given. [{Image src='reaction5573040704696213473.jpg' alt='reaction' caption=''}
- Starting from cyclohex-2-enone and any other reagents needed, how would you prepare the depicted substance? (More than one step may be required.)
- Starting from cyclohex-2-enone and any other reagents needed, how would you prepare the indicated substances? (More than one step may be required.)
- Starting with benzene and any other necessary reagents, design a synthesis of the following compounds.
- What carbonyl starting materials are needed to prepare the below compound using a directed aldol reaction?
- 1) What reagents are needed to produce the following transformation? 2) Outline all steps in the following synthesis.
- Propose a synthesis of methyl p-nitrobenzoate starting with benzene and any other reagents you might need.
- Outline the preparation of the following compounds from the indicated starting materials and any other reagents. a. p-nitroanisole from p-nitrophenol. b. 2-phenoxyethanol from phenol.
- Give the reaction steps required for the synthesis of the following compound. You may use all needed organic and inorganic reagents but must start with the cyclopentanone. The synthesis can be complet
- Provide starting reactant and reagents for the following synthesis. Synthesize the following compound starting with reagents with 3 or fewer carbons:
- Provide the structure of the reactants necessary to prepare the following compound using the Wittig reaction.
- Identify the reagents necessary to prepare each of the following using a Wittig reaction.
- Which reagents are necessary to prepare the following?
- List the reagents or steps needed to form the following compounds.
- Identify the reagents necessary to prepare the compound below using a Wittig reaction.
- What reagents are needed to convert cyclopentene to (a) bromocyclopentane; (b) trans-1,2-dibromocyclopentane; and (c) 3-bromocyclopentene?
- Comment on the dicarbonyl compound that is needed to prepare the given compound by an intramolecular aldol reaction?
- Starting with benzene and any other reagents that you need, synthesize the following compound. (Hint: Use a Suzuki or Heck reaction in your synthesis.)
- Suggest a synthesis for the following compound using the given starting material. Any necessary reagents and solvents can be used.
- Which reagents are necessary to prepare trans-1,2-cyclopentanediol from cyclopentene?
- Show the steps and reagents necessary to prepare the following compound. Use retrosynthetic analysis as a tool to guide your synthesis.
- Suggest a synthesis of the following aromatic molecule. Use the starting material provided and any other reagents necessary.
- Synthesis Show how the following compound could be prepared (synthesized) from the given starting m necessary reagents/organic compounds In the synthesis.
- Determine the reagent(s) required for the bromination of ethylcyclohexene.[{Image src='reactions5926647353234586755.jpg' alt='reaction' caption=''}]
- Write the reagents that would be required to carry out the following synthesis.
- Determine a synthesis of the given compound from acetylene and any other required reagents.
- Outline syntheses of the following compounds starting with the indicated reagents and using any required inorganic reagents.
- What carbonyl starting materials are needed to prepare the given compound using a directed aldol reaction?
- What carbonyl starting materials are needed to prepare the following compound using a directed aldol reaction?
- Provide the appropriate starting materials and reagents needed to form the following compounds via a Fischer esterification: a. 3-ethylpentyl 5-(1,2-dimethylpropyl)decanoate b. 2-ethyl-4,4-dimethylp
- Show the reagents needed to complete the following syntheses.
- Write a synthesis for the following compounds starting from the compound shown and using any reagents/compounds necessary: [{Image src='regant7634869866640681461.jpg' alt='regant' caption=''}]
- 1. What reagents are needed to produce the following tranformation? 2.Outline all steps in the following synthesis.
- Provide the reactant(s) necessary to prepare the following compound.
- Provide the structure of the reactants necessary to prepare the following compound using the Witting reaction.
- How would you synthesize 3-phenylpropanoic acid from one of the compounds shown below and any other necessary reagents?
- Provide the reagent(s) needed for the following transformation. More than one reagent may be needed for each reaction.
- Provide a multi-step synthesis of the following compound using the indicated starting material and any other reagents. [{Image src='react6518513774549172607.jpg' alt='react' caption=''}]
- Show how the following can be made starting with cyclohexanone and other reagents necessary.
- Starting with the given chemicals and any other necessary reagents, show how you would accomplish the following synthetic conversions. More than one step may be needed. Include all reagents and interm
- Show how a Wittig reaction can be used to prepare the following compound. Also, show how the Wittig reagent could be prepared.
- Prepare the following compound using the materials shown. Use any necessary reagents.
- Identify the reagents needed to complete the following reaction:
- Mention the dicarbonyl compound that is needed to prepare the given compound by an intramolecular aldol reaction?
- Provide reagents needed for the following reaction.
- What starting materials are needed to synthesize the given compound using an aldol or similar reaction?
- Design a synthesis for each question below using the starting materials and any other reagents needed. You don't need to show the mechanisms, but do need to show each compound synthesized along the wa
- Deuce the synthesis of the given compound from acetylene and any other required reagents.
- Starting with cyclohexanone, show how to prepare these compounds. In addition to the given starting material, use any additional organic or inorganic reagents that are required (a) 1-Phenylcyclohexene (b) Cyclohexene oxide (c) trans-1,2-Cyclohexanediol
- Devise a synthesis of the following compound from the indicated starting material, organic compounds containing one or two carbons, and any other required reagents.
- Devise a synthesis of the given compound from acetylene and any other required reagents.
- What reagents are needed to complete the following reaction?
- Design a synthesis of the following starting with benzene, phenylacetylene, acetyl chloride, and any other reagents needed.
- Write the(i) reagents and (ii) mechanistic steps associated with the following reaction:
- Find the starting materials that are needed to synthesize the given compound using an aldol or similar reaction?
- Provide reagent(s) needed to synthesize each product using given starting material. Convert 2-methylbutan-1-ol into 2-methylbutanal Convert 1 -hexyne into 2-hexanone
- Synthesize the following molecule from benzaldehyde. Show all steps and reagents used in your synthesis.
- The reagent needed to convert (CH3)2CHCH2COCl to the given compound is ?
- Provide necessary reagents or intermediates for the following reaction sequence.
- How would you prepare cis-2-butene starting from propyne, an alkyl halide, and any other reagents needed? This problem can't be worked in a single step. You will have to carry out more than one reaction.
- Write the starting materials are needed to synthesize the given compound using an aldol or similar reaction?
- Provide the reagents necessary to carry out the following conversion using a malonic ester synthesis.
- Devise a synthesis of the below compound from the indicated starting material. You may use any other needed organic or inorganic reagents.
- Provide the reaction sequence required to convert benzene to the following compound.
- Provide the reagents necessary to carrProvide the reagents necessary to carry out the following conversion [{Image src='img206001397113549478539.jpg' alt='' caption=''}]y out the following conversio
- Synthesize the following product from the give starting compound. More than one step will be required. Any organic or inorganic reagent can be used to carry out the synthesis
- Provide the reagents that are required to complete the following reaction mechanism for the following product.
- Find the reagents necessary to carry out the following conversion.
- Show the synthesis of CH_3CH_2CH_2CH_2CHO by starting with acetylene and any other organic or inorganic compounds. Show all needed reagents.
- Provide the reagents required to complete the following transformation.
- Predict the reactants, reagents and intermediates needed for the following transformation using only the below as your source of carbon. Meaning, you may use any reagent needed, even those with atoms
- Multi-step synthesis: Starting with given compound and using any other reagents of your choice, provide a synthesis for the following compound. Please use reactions that give the desired product as th
- Provide the reagents needed for the following two-step transformation. You will need excess of the second reagent to fully produce the alkyne:
- Frame a synthesis of the given compound from acetylene and any other required reagents.
- Show the steps in preparing the following molecule using a malonic ester synthesis.
- Propose a synthesis for the following compound, with benzene as the starting reagent.
- Deduce the starting materials that are needed to synthesize the given compound using an aldol or similar reaction?
- Identify the appropriate reactants and reagents needed for the following reaction sequence.
- Devise a synthesis of the following compound from cyclohexene and any required organic compounds or inorganic reagents.
- The following molecule was formed by an intramolecular aldol reaction. What dicarbonyl precursor was used for its preparation?
- Show how you would synthesize the following compound using an aldol reaction.
- Frame the alkene needed to start with to prepare the following product?
- Provide reagents to accomplish the following syntheses. Show the product of each formation.
- Identify the reagents necessary to prepare the following compounds using a wittig reaction. [{Image src='tama75905112753351414539.png' alt='' caption=''}]
- Using 1-methylcyclohexane as your starting material, how would you synthesize 1-methylenecyclohexane? Use reaction equations and any reagent necessary.
- Identify the reagents/starting material necessary to make each of the following compounds with an aldol condensation:
- Provide the reagents needed to do the synthesis in 3 steps.
- Outline a reaction sequence for thOutline a reaction sequence for the synthesis of each of the following compounds from the indicated starting material and any other organic or inorganic reagents need
- 1) Please provide the reagents necessary to complete the following transformation. 2) Please provide the reagents required following reaction sequence. Show mechanism
- What reagents would you need for the following transformation? A) H_2, Pd/C B) H_2, lindlar catalyst C) Li, NH_3 D) Na B H_4 E) None of the above
Explore our homework questions and answers library
Browse
by subject