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Alkene (X) (C(5)H(10)) on ozonolysis giv...

Alkene (X) `(C_(5)H_(10))` on ozonolysis gives a mixture of two compounds (Y) and (Z). Compound (Y) gives positive Fehling's test and iodoform test. Compound (Z) does not give Fehling's test but give iodoform test. Name the compound formed when Z reacts with Mg - Hg / `H_(2)O`

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To solve the question step by step, we will analyze the information given and deduce the required compounds and their reactions. ### Step 1: Identify the compounds Y and Z from the ozonolysis of alkene (X) - The alkene (X) has the formula \(C_5H_{10}\). - Upon ozonolysis, it produces two compounds (Y and Z). - Compound (Y) gives a positive Fehling's test and an iodoform test, indicating that it is an aldehyde with a ketomethyl group (a methyl group adjacent to a carbonyl group). - Compound (Z) does not give a Fehling's test but gives an iodoform test, indicating that it is a ketone with a ketomethyl group. ### Step 2: Determine the structure of compound Y - Since Y is an aldehyde and gives a positive iodoform test, it must be an aldehyde with a structure that includes a ketomethyl group. - The simplest structure that fits this description is **butanal** (an aldehyde with four carbons) and a methyl group adjacent to the carbonyl, which gives us **3-pentanone**. ### Step 3: Determine the structure of compound Z - Compound Z is a ketone that gives a positive iodoform test. The only ketone that fits this description and has a ketomethyl group is **acetone** (which is 2-propanone). ### Step 4: Write the ozonolysis reaction - The ozonolysis of the alkene (X) leads to: - Y: 3-pentanone (C4H8O) - Z: Acetone (C3H6O) ### Step 5: Identify the reaction of compound Z (acetone) with Mg-Hg/H2O - When acetone reacts with magnesium amalgam (Mg-Hg) in the presence of water, it undergoes a reduction reaction known as the **pinacol reaction**, leading to the formation of **pinacol**. - The reaction can be summarized as: \[ 2 \text{acetone} \xrightarrow{\text{Mg-Hg/H}_2\text{O}} \text{pinacol} \] ### Step 6: Name the compound formed - The compound formed from the reaction of acetone with Mg-Hg/H2O is **pinacol**. - The IUPAC name of pinacol is **2,3-dimethyl-2,3-butanediol**. ### Final Answer The compound formed when Z (acetone) reacts with Mg-Hg/H2O is **pinacol**, or its IUPAC name is **2,3-dimethyl-2,3-butanediol**. ---
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An alkene 'X' (molecular formula C_(5)H_(10) ) on ozonolysis gives a mixture of two compounds 'Y' and 'Z'. Compound 'Y' gives positive Fehling's test and also forms iodoform on treatement with I_(2)" and "NaOH . Compound 'Z' does not give Fehling's test but forms iodoform. Identify the compounds X, Y and Z. Write the reaction for ozonolysis and formation of iodoform from Y and Z.

An alkene 'A' (molecular formula C_(5)H_(10) ) on ozonolysis gives a mixture of two compounds 'B' and 'C'. Compound 'B' gives positive Fehling's test and also forms iodoform on treatement with I_(2)" and "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.

(a) Carry out the following conversions : (i) pnitrotoluene to 2-bromobenzoic acid (iii) Propanoic acid to acetic acid (b)An alkene with molecular formula C_5H_10 on ozonolysis gives a mixture of two compound B and C .Compound B gives positive Fehling test and also reacts with iodine and NaOH solution. Compound C does not give Fehling solution test but forms iodoform. Identify the compounds A, B and C.

A compound that gives positive iodoform test is

A compound that gives a positive iodofrm test is :

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