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Similar search terms for Ethanoic:
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Why is it called ethanoic acid and not ethanoic acid?
The correct name for the compound CH3COOH is ethanoic acid, not ethanoic acid. This is because the IUPAC naming system for organic compounds uses the suffix "-oic acid" to indicate a carboxylic acid functional group. Therefore, the correct name for CH3COOH follows this naming convention as ethanoic acid.
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What is the reaction of ethanal to ethanoic acid?
The reaction of ethanal to ethanoic acid involves the oxidation of the aldehyde functional group (-CHO) to a carboxylic acid functional group (-COOH). This oxidation reaction typically requires an oxidizing agent, such as potassium dichromate or acidified potassium permanganate, and may be catalyzed by an acid or base. The overall reaction can be represented as: CH3CHO + [O] → CH3COOH, where [O] represents the oxidizing agent.
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How can I differentiate between ethanol, ethanal, and ethanoic acid?
One way to differentiate between ethanol, ethanal, and ethanoic acid is by their chemical structures. Ethanol has the chemical formula C2H5OH and is a primary alcohol. Ethanal, also known as acetaldehyde, has the chemical formula CH3CHO and is an aldehyde. Ethanoic acid, also known as acetic acid, has the chemical formula CH3COOH and is a carboxylic acid. Additionally, their physical properties such as odor, taste, and solubility can also help in distinguishing between them.
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What is the reaction equation of ethanoic acid with lithium?
The reaction equation of ethanoic acid with lithium is as follows: 2CH3COOH + 2Li -> 2CH3COOLi + H2 In this reaction, ethanoic acid (CH3COOH) reacts with lithium (Li) to form lithium ethanoate (CH3COOLi) and hydrogen gas (H2). This is a single displacement reaction where lithium replaces the hydrogen in the ethanoic acid molecule.
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How can I distinguish between ethanol, ethanal, and ethanoic acid?
You can distinguish between ethanol, ethanal, and ethanoic acid by their physical and chemical properties. Ethanol is a colorless liquid with a characteristic odor, and it is flammable. Ethanal, also known as acetaldehyde, is a colorless liquid with a strong, suffocating odor, and it is also flammable. Ethanoic acid, also known as acetic acid, is a clear, colorless liquid with a pungent odor, and it is also flammable. Additionally, you can use chemical tests such as oxidation reactions to differentiate between these compounds.
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Does ethanoic acid donate both protons when it reacts with water?
Yes, ethanoic acid (acetic acid) donates only one proton when it reacts with water. This proton is donated from the carboxylic acid group (-COOH) of ethanoic acid, forming the acetate ion (CH3COO-) and a hydronium ion (H3O+). The second proton from the hydroxyl group (-OH) of ethanoic acid does not dissociate in water.
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Does it matter which structural formula is used for ethanoic acid?
Yes, it does matter which structural formula is used for ethanoic acid. The structural formula provides important information about the arrangement of atoms in the molecule, which can impact its chemical and physical properties. For example, the structural formula can indicate the presence of functional groups, the geometry of the molecule, and its reactivity. Therefore, using the correct structural formula is important for accurately representing the properties and behavior of ethanoic acid in chemical reactions and interactions with other substances.
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What does the octet rule state for ethane, ethanol, and ethanoic acid?
The octet rule states that atoms tend to gain, lose, or share electrons in order to achieve a full outer shell of eight electrons. In ethane (C2H6), each carbon atom forms four single bonds with hydrogen atoms, satisfying the octet rule. In ethanol (C2H5OH), one of the carbon atoms forms a single bond with an oxygen atom, also satisfying the octet rule. In ethanoic acid (CH3COOH), the carbon atom in the carboxyl group forms a double bond with an oxygen atom and a single bond with another oxygen atom, fulfilling the octet rule for both oxygen atoms.
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How can ethanol, ethanoic acid, and sodium hydroxide solution be experimentally differentiated?
Ethanol, ethanoic acid, and sodium hydroxide solution can be experimentally differentiated through a series of simple tests. Ethanol can be distinguished by its characteristic smell and flammability. Ethanoic acid can be identified by its sour taste and its ability to turn blue litmus paper red. Sodium hydroxide solution can be recognized by its slippery feel and its ability to turn red litmus paper blue. Additionally, a chemical reaction with hydrochloric acid can be used to differentiate between the three substances, as ethanol and ethanoic acid will produce a distinct smell when reacted with the acid, while sodium hydroxide solution will not.
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Why does this happen in the reaction of ethanoic acid with calcium carbonate?
This reaction occurs because ethanoic acid (acetic acid) is a weak acid that can react with calcium carbonate, which is a basic compound. When ethanoic acid reacts with calcium carbonate, it forms calcium acetate, carbon dioxide gas, and water. The carbon dioxide gas is released as bubbles, causing the fizzing or effervescence observed during the reaction. This reaction is a classic example of an acid-base reaction, where the acid (ethanoic acid) reacts with the base (calcium carbonate) to form a salt (calcium acetate) and water.
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Why does this occur during the reaction of ethanoic acid with calcium carbonate?
This occurs because ethanoic acid (acetic acid) is a weak acid, and when it reacts with calcium carbonate, it undergoes a neutralization reaction. The calcium carbonate, which is a basic compound, reacts with the ethanoic acid to form calcium acetate, carbon dioxide, and water. The carbon dioxide gas is released as bubbles, causing the fizzing or effervescence during the reaction.
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Why does diluted ethanoic acid react with magnesium in the same way as inorganic acids?
Diluted ethanoic acid, also known as acetic acid, reacts with magnesium in the same way as inorganic acids because it is a weak acid. Despite being an organic acid, it still releases hydrogen gas when it reacts with magnesium, just like inorganic acids. This is because the reaction between the acid and the metal is based on the ability of the acid to donate hydrogen ions, which is a characteristic of all acids, regardless of whether they are organic or inorganic. Therefore, the reaction of diluted ethanoic acid with magnesium follows the same principles as inorganic acids.
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