English

Match the common names given in Column I with the IUPAC names given in Column II. Column I (Common names) Column II (IUPAC names) (i) Cinnamaldehyde (a) Pentanal (ii) Acetophenone (b) - Chemistry

Advertisements
Advertisements

Question

Match the common names given in Column I with the IUPAC names given in Column II.

  Column I
(Common names)
  Column II
(IUPAC names)
(i) Cinnamaldehyde (a) Pentanal
(ii) Acetophenone (b) Prop-2-enal
(iii) Valeraldehyde (c) 4-Methylpent-3-en-2-one
(iv) Acrolein (d) 3-Phenylprop-2-enal
(v) Mesityl oxide (e) 1-Phenylethanone
Match the Columns

Solution

  Column I
(Common names)
  Column II
(IUPAC names)
(i) Cinnamaldehyde (d) 3-Phenylprop-2-enal
(ii) Acetophenone (e) 1-Phenylethanone
(iii) Valeraldehyde (a) Pentanal
(iv) Acrolein (b) Prop-2-enal
(v) Mesityl oxide (c) 4-Methylpent-3-en-2-one

Explanation:

(Common names) Structure (IUPAC names)
(i) Cinnamaldehyde 3-Phenylprop-2-enal
(ii) Acetophenone 1-Phenylethanone
(iii) Valeraldehyde Pentanal
(iv) Acrolein Prop-2-enal
(v) Mesityl oxide 4-Methylpent-3-en-2- one
shaalaa.com
  Is there an error in this question or solution?
Chapter 12: Aldehydes, Ketones and Carboxylic Acids - Multiple Choice Questions (Type - I) [Page 174]

APPEARS IN

NCERT Exemplar Chemistry [English] Class 12
Chapter 12 Aldehydes, Ketones and Carboxylic Acids
Multiple Choice Questions (Type - I) | Q 38 | Page 174

Video TutorialsVIEW ALL [1]

RELATED QUESTIONS

Write the product in the following reaction


Write the chemical equations to illustrate the following name reactions : Rosenmund reduction


Esters react with DIBAL-H to produce:


The oxidation of toluene to benzoic acid can be stopped at the aldehyde stage to give benzaldehyde. The reagent used for the purpose is one of the following.


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 strongest base among the following


Aldehydes are the first oxidation products of ______.


Convert the following:

Benzoic acid to Benzaldehyde


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.


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×