Keton Samenvattingen, Aantekeningen en Examens
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![EXPH 240 Exam 4 Endocrine System Questions & Answers Already Graded A+](/docpics/5409743/664ed85ba4ca3_5409743_121_171.jpeg)
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EXPH 240 Exam 4 Endocrine System Questions & Answers Already Graded A+
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dips/o - thirst 
gluc/o, glucos/om glyc/o - glucose 
hormon/o - hormone 
ket/o, keton/o - ketone bodies 
pancreat/o - pancreas 
thym/o - thymus gland 
thyr/o, thyroid/o - thyroid gland (shield) 
adrenal glands - located on the superior surface of each kidney; the adrenal cortez secretes 
steroid hormones, and the adrenal medulla secretes epinephrine and norepinephrine 
steroid hormones - hormones secreted by the adrenal cortex 
catecholamines - hormones secreted by the adrenal medulla that affec...
![LMR OC 3: Aldehydes and Ketones 2 Questions and answers](/docpics/4932642/661073bf4e9cc_4932642_121_171.jpeg)
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LMR OC 3: Aldehydes and Ketones 2 Questions and answers
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Acidity of α-Hydrogen: Carbonyl 
α-carbon: Next to the carbonyl carbon. 
α-Hydrogen: H of alpha carbons 
Oxygen pulls electron density out of these C-H bonds so it's easier to deprotonate the 
α-carbon of aldehydes/ketones. 
How do you increase the acidity of α-Hydrogen? 
- Resonance stability provided by the conjugate base 
- Resonance can stabilize enolate intermediate, since negative charge is distributd to 
more EN oxygen atom 
- Alpha hydrogen can easily deprotonate in basic solutions...
Organic Chemistry 10th Edition by Francis Carey - Test Bank
![Chemical properties of Aldehydes and Ketones Reactions common to both Aldehydes and Ketones The difference between an Aldehyde and a Ketone is the position of the C=O (Carbonyl group). Aldehyde – always on a carbon at the end of the chain Ketone – Always](/docpics/5326735/66464ddfeeeda_5326735_121_171.jpeg)
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Chemical properties of Aldehydes and Ketones Reactions common to both Aldehydes and Ketones The difference between an Aldehyde and a Ketone is the position of the C=O (Carbonyl group). Aldehyde – always on a carbon at the end of the chain Ketone – Always
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Chemical properties of Aldehydes and Ketones 
Reactions common to both Aldehydes and Ketones 
The difference between an Aldehyde and a Ketone is the position of 
the C=O (Carbonyl group). 
Aldehyde – always on a carbon at the 
end of the chain Ketone – Always on a 
carbon at middle carbon of the chain 
1. BOTH Aldehydes and Ketones can be reduced 
Aldehyde reduced to Primary 
Alcohol Reducing agent = Sodium 
tetrahydroborate III (NaBH4) 
Ketone reduced to Secondary Alcohol 
Reduction 
Oxid...
![Chemical properties of Aldehydes and Ketones Reactions common to both Aldehydes and Ketones The difference between an Aldehyde and a Ketone is the position of the C=O (Carbonyl group). Aldehyde – always on a carbon at the end of the chain Ketone – Always](/docpics/5513331/665cd21caa4e5_5513331_121_171.jpeg)
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Chemical properties of Aldehydes and Ketones Reactions common to both Aldehydes and Ketones The difference between an Aldehyde and a Ketone is the position of the C=O (Carbonyl group). Aldehyde – always on a carbon at the end of the chain Ketone – Always
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Chemical properties of Aldehydes and Ketones 
Reactions common to both Aldehydes and Ketones 
The difference between an Aldehyde and a Ketone is the position of 
the C=O (Carbonyl group). 
Aldehyde – always on a carbon at the 
end of the chain Ketone – Always on a 
carbon at middle carbon of the chain 
1. BOTH Aldehydes and Ketones can be reduced 
Aldehyde reduced to Primary 
Alcohol Reducing agent = Sodium 
tetrahydroborate III (NaBH4) 
Ketone reduced to Secondary Alcohol 
Reduction 
Oxid...
![NR 442 Choose a compound that is classified as an ether, aldehyde, ketone, ester, or alcoh](/docpics/5647138/666db943bf1b1_5647138_121_171.jpeg)
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NR 442 Choose a compound that is classified as an ether, aldehyde, ketone, ester, or alcoh
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NR 442 Choose a compound that is classified as an ether, aldehyde, ketone, ester, or alcoh NR 442 Choose a compound that is classified as an ether, aldehyde, ketone, ester, or alcohol, or amide. Report on important applications of this compound using at least one outside source. Next, write the condensed structural formula of a simple molecule with an ether, aldehyde, ketone, ester, or alcohol functional group for your peers to name (do not give away the answer!).One compound that is classified...
![Naming and Identifying Organic Molecules (Carboxylic acids, Aldehydes, Ketones, Alcohols, Alkanes, Alkenes) Exam 2023-2024](/docpics/3015983/64a560e859503_3015983_121_171.jpeg)
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Naming and Identifying Organic Molecules (Carboxylic acids, Aldehydes, Ketones, Alcohols, Alkanes, Alkenes) Exam 2023-2024
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Naming and Identifying Organic 
Molecules (Carboxylic acids, Aldehydes, 
Ketones, Alcohols, Alkanes, Alkenes) 
Exam 2023-2024 
HCOOH (IUPAC) - Correct Answer-methanoic acid 
CH3-COOH (IUPAC) - Correct Answer-ethanoic acid 
CH3-CH2-COOH (IUPAC) - Correct Answer-propanoic acid 
CH3-CH2-CH2-COOH (IUPAC) - Correct Answer-butanoic acid 
CH3-CH2-CH2-CH2-COOH (IUPAC) - Correct Answer-pentanoic acid 
HCHO/ CH2O (IUPAC) - Correct Answer-methanal 
CH3-CHO (IUPAC) - Correct Answer-ethanal 
CH3-CH2-CHO (I...
![Naming and Identifying Organic Molecules (Carboxylic acids, Aldehydes, Ketones, Alcohols, Alkanes, Alkenes) Exam 2023-2024](/docpics/3005497/64a3030ecdb16_3005497_121_171.jpeg)
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Naming and Identifying Organic Molecules (Carboxylic acids, Aldehydes, Ketones, Alcohols, Alkanes, Alkenes) Exam 2023-2024
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Naming and Identifying Organic 
Molecules (Carboxylic acids, Aldehydes, 
Ketones, Alcohols, Alkanes, Alkenes) 
Exam 2023-2024 
HCOOH (IUPAC) - Correct Answer-methanoic acid 
CH3-COOH (IUPAC) - Correct Answer-ethanoic acid 
CH3-CH2-COOH (IUPAC) - Correct Answer-propanoic acid 
CH3-CH2-CH2-COOH (IUPAC) - Correct Answer-butanoic acid 
CH3-CH2-CH2-CH2-COOH (IUPAC) - Correct Answer-pentanoic acid 
HCHO/ CH2O (IUPAC) - Correct Answer-methanal 
CH3-CHO (IUPAC) - Correct Answer-ethanal 
CH3-CH2-CHO (I...
Aldehydes and Ketones Notes
![A* GRADE AQA A-Level Chemistry: Organic - Aldehydes and Ketones (3.3.8)](/docpics/64500bbd84756_2539075.jpg)
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A* GRADE AQA A-Level Chemistry: Organic - Aldehydes and Ketones (3.3.8)
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I achieved a high A* Grade in my final A-Level exams using these notes!!! 
I believe you can achieve an A* if you can memorise these notes! Simply use blurting, a method of active recall, to write everything you remember from the notes, then identify the parts you couldn’t remember, then repeat until you can remember it all! If you can do that, you’ve got an A* in the bag! 
They are clear, concise, and are laid out according to the specification; there is no information missing or in excess...
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