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In a testcross involving F(1) dihybrid f...

In a testcross involving `F_(1)` dihybrid flies, more parental-type offsping were produces than the recombinant-type offspring. This indicates

A

Both of the characters are controlled by more than-one gene

B

The two genes are located on two different chromosomes.

C

Chromosomes failed to separate during meiosis

D

The two genes are linked and present on the same chromosome

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In peas, tallness is dominant over dwarfness, and red colour of flowers is dominant over the white colour. When a tall plant bearing red flowers was pollinated by a dwarf plant bearing white flowers, the different phenotypic groups were obtained in the progeny in numbers mentioned against them Tall, Red = 138 Tall, White = 132 Dwarf, Red = 136 Dwarf, White = 128 Mention the genotypes of the two parents and of the types of four offspring

Di-tert-glycols rearrange in the presence of acid to give alpa -tertiary ketones. The trivial name of the simplest glycol of this type is pinacol, and this type of reaction therefore is named pinacol rearrangement (in this specific case, the reaction is called a pinacol-pinacolone rearrangement). The rearrangement involves 4 steps. one of the hydroxyl groups is protonated in the first step. A molecule of water is eliminated in the second step and a tertiary carbocation is formed. The carbocation rearranges in the third step into a more stable carboxonium ion via a [1,2] rearrangement. In the last step, the carboxonium ion is deprotonated and the product ketone is obtained. How many products obtained in above reaction?

Knowledge Check

  • Two genes 'A' and 'B' are linked. In a dihybrid cross involving these two genes, the F_1 heterozygote is crossed with homozygous recessive parental type (aa bb). What would be the ratio of offspring in the next generation ?

    A
    1:1:1:1
    B
    9:3:3:1
    C
    `3:1`
    D
    `1:1`
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    Give reasons: (i) Zirconium (Z = 40) and Hafnium (Z = 72) have almost similar atomic radii. (ii) d-block elements exhibit more oxidation states than f-block elements. (iii) The enthalpies of atomization of the transition metals are high (iv) The variation in oxidation states of transition metals is of different type from that of the non transition metals. (v) Orange solution of potassium dichromate turns yellow on adding sodium hydroxide to it.

    Di-tert-glycols rearrange in the presence of acid to give alpa -tertiary ketones. The trivial name of the simplest glycol of this type is pinacol, and this type of reaction therefore is named pinacol rearrangement (in this specific case, the reaction is called a pinacol-pinacolone rearrangement). The rearrangement involves 4 steps. one of the hydroxyl groups is protonated in the first step. A molecule of water is eliminated in the second step and a tertiary carbocation is formed. The carbocation rearranges in the third step into a more stable carboxonium ion via a [1,2] rearrangement. In the last step, the carboxonium ion is deprotonated and the product ketone is obtained.

    Di-tert-glycols rearrange in the presence of acid to give alpa -tertiary ketones. The trivial name of the simplest glycol of this type is pinacol, and this type of reaction therefore is named pinacol rearrangement (in this specific case, the reaction is called a pinacol-pinacolone rearrangement). The rearrangement involves 4 steps. one of the hydroxyl groups is protonated in the first step. A molecule of water is eliminated in the second step and a tertiary carbocation is formed. The carbocation rearranges in the third step into a more stable carboxonium ion via a [1,2] rearrangement. In the last step, the carboxonium ion is deprotonated and the product ketone is obtained.

    Di-tert-glycols rearrange in the presence of acid to give alpa -tertiary ketones. The trivial name of the simplest glycol of this type is pinacol, and this type of reaction therefore is named pinacol rearrangement (in this specific case, the reaction is called a pinacol-pinacolone rearrangement). The rearrangement involves 4 steps. one of the hydroxyl groups is protonated in the first step. A molecule of water is eliminated in the second step and a tertiary carbocation is formed. The carbocation rearranges in the third step into a more stable carboxonium ion via a [1,2] rearrangement. In the last step, the carboxonium ion is deprotonated and the product ketone is obtained. What is R.D.S. of pinacol-pinacolone rearrangement?

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