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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom. p-Nitrobenzaldehyde - Chemistry

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प्रश्न

How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.

p-Nitrobenzaldehyde

रासायनिक समीकरण/संरचनाएँ
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उत्तर

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अध्याय 8: Aldehydes, Ketones and Carboxylic Acids - Exercises [पृष्ठ २५६]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
अध्याय 8 Aldehydes, Ketones and Carboxylic Acids
Exercises | Q 8.14 (v) | पृष्ठ २५६

संबंधित प्रश्न

Write the product in the following reaction


Write the product in the following reaction:


Write the structure of the product of the following reaction:


Write the reaction involved in the Stephen reduction


Aldehydes are prepared by reducing nitriles to corresponding imines with stannous chloride in the presence of hydrochloric acid. This reaction is called:


The oxidation of toluene to benzoic acid can be done using which of the following reagents.


Can Gatterman-Koch reaction be considered similar to Friedel Craft’s acylation? Discuss.


Match the example given in Column I with the name of the reaction in Column II.

  Column I
(Example)
  Column II
(Reaction)
(i) \[\begin{array}{cc}
\phantom{...}\ce{O}\phantom{..............................}\ce{O}\phantom{}\\
\phantom{...}||\phantom{..............................}||\phantom{}\\
\ce{CH3 - C - Cl + H2 ->[Pd - C/BasO4] CH3 - C - H}
\end{array}\]
(a) Friedel Crafts acylation
(ii) (b) HVZ reaction
(iii) (c) Aldol condensation
(iv) \[\begin{array}{cc}
\ce{R - CH2 - COOH ->[Br/Red P] R - CH - COOH}\\
\phantom{.....................}|\\
\phantom{.......................}\ce{Br}
\end{array}\]
(d) Cannizaro’s reaction
(v) \[\ce{CH3 - CN ->[(i) SnCl2/HCl][(ii) H2O/H+] CH3CHO}\] (e) Rosenmund’s reductio
(vi) \[\ce{2CH3CHO ->[NaOH] CH3 - CH = CHCHO}\] (f) Stephen’s reaction

An alkene ‘A’ (Mol. formula \[\ce{C5H10}\]) on ozonolysis gives a mixture of two compounds ‘B’ and ‘C’. Compound ‘B’ gives positive Fehling’s test and also forms iodoform on treatment with \[\ce{I2}\] and \[\ce{NaOH}\]. Compound ‘C’ does not give Fehling’s test but forms iodoform. Identify the compounds A, B and C. Write the reaction for ozonolysis and formation of iodoform from B and C.


The general formula CnH2NO2 could be for open chain


The intermediate compound ‘X’ in the following chemical reaction is:


The oxidation of toluene to benzaldehyde by chromyl chloride is called ______.


Convert the following:

Benzoic acid to Benzaldehyde.


Explain the following reactions:

Stephan reaction


Reagent used to convert allyl alcohol to acrolein is ______.


Assertion (A): Strong oxidising agents oxidise toluene and its derivatives to benzoic acids.

Reason (R): It is possible to stop the oxidation of toluene at the aldehyde stage with suitable reagents.

Select the most appropriate answer from the options given below:


An organic compound with molecular formula \[\ce{C7H7NO2}\] exists in three isomeric forms, the isomer ‘A’ has the highest melting point of the three. ‘A’ on reduction gives compound ‘B’ with molecular formula \[\ce{C7H9N}\]. ‘B’ on treatment with \[\ce{NaNO2/HCl}\] at 0-5° C to form compound ‘C’. On treating C with \[\ce{H3PO2}\], it gets converted to D with formula \[\ce{C7H8}\], which on further reaction with \[\ce{CrO2Cl2}\] followed by hydrolysis forms ‘E’ \[\ce{C7H6O}\]. Write the structure of compounds A to E. Write the chemical equations involved.


Account for the following:

Reduction of nitrobenzene using Fe and HCl is preferred over Sn and HCl.


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