Given reaction sequence:
C6H12O6 → (i) OH−/H2O, Δ → (ii) H3O+ → H + 1 → CrO3/H+
Step-by-step explanation:
Step 1: C6H12O6 → Under basic hydrolysis and heating (OH−/H2O, Δ), glucose undergoes degradation reactions (retro-aldol type cleavages) that break it into smaller fragments such as aldehydes and carboxylic acids.
Step 2: Acidification (H3O+) causes the intermediate products to be protonated, stabilizing them for further reaction.
Step 3: Reaction with CrO3/H+ (oxidation) selectively oxidizes aldehyde groups into carboxylic acids, forming esters when alcohols are also present.
Target Compound G: The expected product is an ester with the structure CH3CH2COOCH2CH2CH3 – this matches with the systematic breakdown of glucose followed by esterification and oxidation steps.
Correct option: (C): CH3CH2COOCH2CH2CH3
(i) Explain Aldol condensation with example.
(ii) How are the following conversions achieved:
(a) Benzene Benzaldehyde, (b) Ethanoic acid ethanol.
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Manufacturers supply a zener diode with zener voltage \( V_z=5.6\,\text{V} \) and maximum power dissipation \( P_{\max}=\frac14\,\text{W} \). This zener diode is used in the circuit shown. Calculate the minimum value of the resistance \( R_s \) so that the zener diode will not burn when the input voltage is \( V_{in}=10\,\text{V} \). 
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Aldehydes, Ketones, and Carboxylic Acids are carbonyl compounds that contain a carbon-oxygen double bond. These organic compounds are very important in the field of organic chemistry and also have many industrial applications.
Aldehydes are organic compounds that have the functional group -CHO.
Preparation of Aldehydes
Acid chlorides are reduced to aldehydes with hydrogen in the presence of palladium catalyst spread on barium sulfate.
Ketones are organic compounds that have the functional group C=O and the structure R-(C=O)-R’.
Preparation of Ketones
Acid chlorides on reaction with dialkyl cadmium produce ketones. Dialkyl cadmium themselves are prepared from Grignard reagents.
Carboxylic acids are organic compounds that contain a (C=O)OH group attached to an R group (where R refers to the remaining part of the molecule).
Preparation of Carboxylic Acids
Primary alcohols are readily oxidized to carboxylic acids with common oxidizing agents such as potassium permanganate in neutral acidic or alkaline media or by potassium dichromate and chromium trioxide in acidic media.