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The NCERT Class 12 Chemistry chapter 11 notes are very important for the exam. Students will study about the preparation, characteristics, and reactivity of alcohols, phenols, and ethers in this chapter. This chapter addresses some of the most fundamental topics in organic chemistry, as well as their industrial applications. Integrating ch 11 Chemistry Class 12 notes into one's study routine will help students in better comprehension of alcohols, phenols, and ethers, enhancing problem-solving skills and analytical abilities. CBSE Class 12 Chemistry Ch 11 notes provide a structured overview of the syllabus, guiding students through essential topics and highlighting crucial points for effective revision.
Comprehensive reading of alcohols, phenols and ethers notes class 12 is essential for gaining a thorough understanding of this segment of organic chemistry. cbse class 12 chemistry ch 11 notes provide a brief synopsis of the chapter for quick preparation of CBSE board exams and school-based annual examinations.
Also, students can refer,
Alcohols and phenols are classed as monohydric, dihydric, trihydric, or polyhydric depending on how many hydroxyl groups they have in their molecules: one, two, three, or many, respectively
Alcohols with the OH group connected to a primary, secondary, or tertiary carbon atom are known as primary (1°), secondary (2°), and tertiary (3°) alcohols.
Allylic alcohol is made up of an -OH group attached to an sp3 hybridized carbon next to a carbon carbon double bond, whereas benzylic alcohol is made up of an -OH group attached to an sp3 hybridized carbon close to an aromatic ring. Alcohols having -OH group bonded to carbon-carbon double bond is called vinylic alcohol
Alcohols have sp3 hybridized oxygen atoms and hybrid atomic orbitals in a tetrahedral configuration. The R group determines the value of the LROH bond angle. Due to lone pair repulsion, this angle for of methyl alcohol is (C – O – H) 108.9°.The -OH group in phenols is connected to sp2 hybridized carbon, giving the C – O bond a partial double bond nature.
From alkenes
This reaction is in accordance with Markonikov's rule, through acid catalyzed hydration.
CH3CH=CH2 + H2O → CH3-CH(OH) - CH3
By hydroboration-oxidation
By reduction of aldehydes and ketones
RCHO + H2 → R CH2OH
By reduction of carboxylic acids
From Grignard reagents
From haloarenes
From benzenesulfonicacid
From diazonium salts
From cumenes
NCERT Class 12 Chemistry Chapter 11 Notes: Topic 5
Lower alcohols are colourless liquids, C5–C11 alcohols are oily liquids, and C12 and higher alcohols are waxy solids. Alcohols are miscible with water because their hydroxyl groups can form H-bonds with water. With increasing molecular mass, solubility decreases. Because polar molecules have intermolecular hydrogen bonding, the boiling points of alkanes are greater than expected.
These are colourless liquids or crystalline solids that turn coloured over time due to gradual oxidation in the presence of air. Carboxylic acid is another name for phenol. Phenols establish intermolecular H-bonds with other phenol molecules and with water due to the presence of a polar -OH bond.
Acidity of alcohols and phenols
Reaction with metals
Acidity of alcohols
The polar nature of the OH bond causes the acidity of alcohols.
Order of acidity
Primary > Secondary Tertiary
Alcohols are weaker acids than water
Acidity of phenols
Because the phenoxide ion is stabilized through resonance, phenol is more acidic than alcohols. The presence of an electron withdrawing group raises phenol's acidity by stabilizing the phenoxide ion, whereas the presence of an electron releasing group lowers phenol's acidity by destabilizing the phenoxide ion.
Esterification
Ar/R-OH + (RCO,)2O + H+↔ Ar/ROCOR, + RCOOH
R/ArOH + R,COCl Pyridine→ R/ArOCOR, + HCl
Reaction with hydrogen halides
ROH + HX yields→ RX + H2O
Dehydration
Alcohols H+, Heat→ Alkene + H2O
Order of reaction
Tertiary > Secondary > Primary
Oxidation
Alcohol Acidified KMnO4→ Carboxylic acid
RCH2OH Oxidation→ RCHO yields→ RCOOH
Reactions of phenol
Halogenation
Nitration
Reimer-Tiemann reaction
Kolbe’s reaction
Reaction with zinc dust
Oxidation
Methanol (CH3OH)
Wood-spirit is another name for it. It is a clear liquid with no discernible colour. It reaches a temperature of 337 degrees Fahrenheit when it boils. It is extremely poisonous. Even little doses can cause blindness, and excessive doses can even result in death
Preparation
CO + 2H2 ZnO-Cr2O3,200-300 atm,573-673 K→ CH3OH
Uses: Paints, varnishes, and other products use it as a solvent.It can be used to make formaldehyde.
Ethanol (C2H5OH)
It is known as denatured spirit when combined with CuSO4 and pyridine.It is a colourless liquid having boiling point 351 K
Preparation
C12H22O11 + H2O Invertase→ C6H12O6 Glucose+ C6H12O6 Fructose
C6H12O6 Zymase→ 2 C2H5OH + 2 CO2
Uses: It is a good solvent, Sterilization of surgical tools in laboratories and hospitals.
By dehydration of alcohols
CH3CH2OH+ H2SO4,443 K→ CH2= CH2
CH3CH2OH + H2SO4,413 K→ C2H5OC2H5
Williamson synthesis
R-X + R-O-Na yields→ R-O-R + NaX
Since ethers' C-O bonds are polar, they have a net dipole moment. Their boiling points are equivalent to alkanes with similar molecular weights, although they are lower than alcohols. It's because ethers don't have H-bonding. Ether miscibility with water is similar to that of alcohols of same molar mass. It's because ethers, like alcohols, can make H-bonds with water.
Cleavage of C-O bonds
R-O-R + HX yields→ RX + R-OH
R-OH + HX yields R-X + H2O
R-O-R + HX yields→ R-X + R-OH
Electrophilic substitution reactions
Halogenation
Friedel craft’s reaction
Nitration
Significance of NCERT Class 12 Chemistry Chapter 11 Notes
Alcohols, Phenols and Ethers class 12 notes provides significant insights for board exams, and competitive exams like JEE and NEET. Class 12 chemistry chapter 10 notes can help you grasp the fundamental principles. This chapter is also useful for entrance exams and competitive exams like VITEEE, BITSAT, JEE Main Core, NEET, etc. As a result, knowledge of that chapter becomes much more important. Class 12 Chemistry chapter 11 notes make it easy to go over the entire chapter 11 in a few minutes. One of the best exam-day strategies given by lecturers is to take Alcohols, Phenols and Ethers Class 12 notes. Students can study offline by downloading chemistry class 12 chapter 11 notes pdf .
Ans- Acidity of alcohols, esterification, oxidation, dehydration, etc are discussed in Class 12 Chemistry chapter 11 notes.
Ans-. Classification of alochols and phenols, preparation of alcohols,phenols and ethers , physical and chemical properties of alcohols , phenols and ethers etc are covered in NCERT notes for Class 12 Chemistry chapter 11.
Ans- One or more hydroxyl groups are connected to a saturated carbon atom in alcohols. A hydroxyl group is linked to an aromatic hydrocarbon system in phenols.
Ans- In alcohols a hydroxyl group is attached to a saturated carbon atom in alcohol, which is an organic molecule. Phenol is an organic compound formed when a hydrogen atom in a benzene molecule is replaced by a -OH group. Ether is an organic molecule composed of two aryl or alkyl groups joined by an oxygen atom. This is mentioned in Class12 Alcohols , phenols and ethers notes.
Ans- Fats, oils, waxes, resins, dyers, gums, and other materials employ ethers as a solvent. Alcohol is a key component in alcoholic beverages. They're also used in the ink, medicine, and ink industries etc. Antiseptic properties of phenols are widely used in pharmaceuticals. Alcohols, phenols, and ether are important ingredients in detergents, antiseptics, and scents. More details are available in Alcohols, phenols and ethers Class 12 pdf download.
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As per latest 2024 syllabus. Physics formulas, equations, & laws of class 11 & 12th chapters
As per latest 2024 syllabus. Chemistry formulas, equations, & laws of class 11 & 12th chapters
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