Electrophillic Study guides, Class notes & Summaries
Looking for the best study guides, study notes and summaries about Electrophillic? On this page you'll find 17 study documents about Electrophillic.
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OCR A-Level Chemistry Paper 2 2022 ALL ANSWERS 100% CORRECT GUARANTEED GRADE A+
- Exam (elaborations) • 11 pages • 2023
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What is an alkene and its general formula? 
It is an unsaturated hydrocarbon with a least one C=C bond. General formula is CnH2n 
What is a sigma bond? σ 
single covalent bond formed when two s orbitals overlap. High electron density 
What is a pi bond? 
sideways overlap of p orbitals that occur in a double or triple bond. Much weaker than sigma, low bond enthalpy and lower electrostatic attraction 
Is an alkane or an alkene more reactive? 
Alkene. contains both sigma and pi bonds with high ele...
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Chemical properties of Aldehydes and Ketones
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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 Oxidisatio...
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AQA A-LEVEL CHEMISTRY PAPER 2MARKING SCHEME JUNE 2022
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AQA A-LEVEL CHEMISTRY PAPER 2MARKING SCHEME JUNE 2022 
AQA A-LEVEL CHEMISTRY PAPER 2MARKING SCHEME JUNE 2022 
 
 
 
 
 
 
 
 
 
A-level 
CHEMISTRY 
7405/2 
Paper 2 Organic and Physical Chemistry 
Mark scheme 
June 2019 
Version: 1.0 Final 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
*196A74052/MS* 
 
 
 
 
 
 
Mark schemes are prepared by the Lead Assessment Writer and considered, together with the relevant questions, by a panel of subject teachers. This mark scheme in...
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Substitution Reaction class notes Chemistry
- Class notes • 26 pages • 2023
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Substitution Reaction class notes include-Electrophillic Substitution Reaction,Nucleophillic Substitution Reaction,Free Radical Reaction,Riemar Tiemann Reaction,Friedal Craft Reaction,Kolbe Reaction,SN1,SN2,SNAE,HVZ Reaction
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Addition Reaction NCERT Covered notes
- Class notes • 32 pages • 2023
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Addition Reaction high quality notes,topics covered- electrophillic addition reaction,nucleophillic addition reaction,free radical addition reaction and some include fehling reaction,tollen reaction,benedict test,schiff test
And that's how you make extra money
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Chemical properties of Aldehydes and Ketones Reactions common to both Aldehydes and Ket
- Exam (elaborations) • 45 pages • 2024
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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 Oxidisatio...
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Chemical properties of Aldehydes and Ketones
- Exam (elaborations) • 45 pages • 2024
-
- $12.49
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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 Oxidisatio...
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Chemical properties of Aldehydes and Ketones Reactions common to both Aldehydes and Ketones
- Exam (elaborations) • 45 pages • 2024
-
- $11.49
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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 Oxidisatio...
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Chemical properties of Aldehydes and Ketones
- Exam (elaborations) • 45 pages • 2024
-
- $9.49
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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 
 ...
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Chemical properties of Aldehydes and Ketones
- Exam (elaborations) • 45 pages • 2024
-
- $10.99
- + learn more
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 Oxidisation ...
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