Assertion : The epiphytes use the trees only for attachment and manufacture their own food by photosynthesis.
Reason : Commensalism results in negative effects on the growth and survival of one or both of the populations.

Assertion: Cheese is one of the oldest food items in which microbes are used. Reason: Different varieties of cheese are known by their charateristic texture, flavour and taste, the specificity coming from the microbes were used. 1)If both Assertion & Reason are true and the reason is the correct explanation of the assertion, then mark (1) 2) If both Assertion & Reason are true but the reason is not the correct explanation of the assertion, then mark (2). 3) If Assertion is true statement but Reaosn is false, then mark (3). 4) If both Assertion and Reason are false statements, then mark (4).

These questions consist of two statements each,printed as Assertion and Reason.While asnwering these questions you are required to chose any one of the following four responses. If both Assertion and Reason are true and Reason in correct explanation of Assertion. If both assertion and Reason are true but reason is not correct explanation of Assertion. If Assertion is true but Reason is false. If both Assertion and Reason are false. Assertion: C_4 plnats form food more rapidly more efficinety in photosynthesis than C_3 plants. REason: C_4 plants have a shorter CO_2 fixation cycle.

The electronic displacements in covalent bonds may occur either in the ground state under the influence of an atom or a substituent group or in presence of an appropriate attacking reagent. As a result of these electron displacements, centres of different electron densities are created and these centres are susceptible to attack by the reagents. These electron displacements occur through inductive electromeric, resonance and hyperconjugation effects. Whereas inductive effect involves displacement of sigam -electrons towards the substituent, resonance effect involves delocalization of pi- electrons transmitted through the chain and both are permanent effect. Electromeric effect is the complete transfer of a shared pair of pi - electrons to one of the atoms joined by a multiple bond on the demand of an attacking reagent. Hyperconjugation effects on the other hand involve delocalization of sigma -electrons of C-H bond of an alkyl group directly attached to an atom of unsaturated system (i.e., sigma-pi -conjugation). Both inductive and hyperconjugation effects can be used to explain the stability of carbocations and free radicals which follow the stability order : 3^(@)gt2^(@)gt1^(@) . The stability or carbanions, however, follows the reverse order. An organic reaction occurs through making and breaking of bonds. The breaking of a covalent bond may occur either homolytic leading to the formation of free radicals or heterolytic forming positively (carbocations) or negatively (carbanions) charged species. Most of the attacking reagents carry either a positive or a negative charge. The positively charged species with electron deficient centre or neutral species (free radicals, carbenes, nitrene) are collectively called electrophiles, while negatively charged species with electron rich centre or neutral species (like water, alcohol, ammonia, etc.) are called nucleophiles. Out of the following series, the one containing only electrophiles is:

The electronic displacements in covalent bonds may occur either in the ground state under the influence of an atom or a substituent group or in presence of an appropriate attacking reagent. As a result of these electron displacements, centres of different electron densities are created and these centres are susceptible to attack by the reagents. These electron displacements occur through inductive electromeric, resonance and hyperconjugation effects. Whereas inductive effect involves displacement of sigam -electrons towards the substituent, resonance effect involves delocalization of pi- electrons transmitted through the chain and both are permanent effect. Electromeric effect is the complete transfer of a shared pair of pi - electrons to one of the atoms joined by a multiple bond on the demand of an attacking reagent. Hyperconjugation effects on the other hand involve delocalization of sigma -electrons of C-H bond of an alkyl group directly attached to an atom of unsaturated system (i.e., sigma-pi -conjugation). Both inductive and hyperconjugation effects can be used to explain the stability of carbocations and free radicals which follow the stability order : 3^(@)gt2^(@)gt1^(@) . The stability or carbanions, however, follows the reverse order. An organic reaction occurs through making and breaking of bonds. The breaking of a covalent bond may occur either homolytic leading to the formation of free radicals or heterolytic forming positively (carbocations) or negatively (carbanions) charged species. Most of the attacking reagents carry either a positive or a negative charge. The positively charged species with electron deficient centre or neutral species (free radicals, carbenes, nitrene) are collectively called electrophiles, while negatively charged species with electron rich centre or neutral species (like water, alcohol, ammonia, etc.) are called nucleophiles. Which of the following groups has highest inductive effect?

The electronic displacements in covalent bonds may occur either in the ground state under the influence of an atom or a substituent group or in presence of an appropriate attacking reagent. As a result of these electron displacements, centres of different electron densities are created and these centres are susceptible to attack by the reagents. These electron displacements occur through inductive electromeric, resonance and hyperconjugation effects. Whereas inductive effect involves displacement of sigam -electrons towards the substituent, resonance effect involves delocalization of pi- electrons transmitted through the chain and both are permanent effect. Electromeric effect is the complete transfer of a shared pair of pi - electrons to one of the atoms joined by a multiple bond on the demand of an attacking reagent. Hyperconjugation effects on the other hand involve delocalization of sigma -electrons of C-H bond of an alkyl group directly attached to an atom of unsaturated system (i.e., sigma-pi -conjugation). Both inductive and hyperconjugation effects can be used to explain the stability of carbocations and free radicals which follow the stability order : 3^(@)gt2^(@)gt1^(@) . The stability or carbanions, however, follows the reverse order. An organic reaction occurs through making and breaking of bonds. The breaking of a covalent bond may occur either homolytic leading to the formation of free radicals or heterolytic forming positively (carbocations) or negatively (carbanions) charged species. Most of the attacking reagents carry either a positive or a negative charge. The positively charged species with electron deficient centre or neutral species (free radicals, carbenes, nitrene) are collectively called electrophiles, while negatively charged species with electron rich centre or neutral species (like water, alcohol, ammonia, etc.) are called nucleophiles. The decreasing order of basic strength in underset("(I)")(C_(6)H_(5)NH_(2))," "underset("(II)")((C_(6)H_(5))_(2)NH)," "underset("(III)")(CH_(3)NH_(2))," "underset("(IV)")(NH_(3)) is:

The electronic displacements in covalent bonds may occur either in the ground state under the influence of an atom or a substituent group or in presence of an appropriate attacking reagent. As a result of these electron displacements, centres of different electron densities are created and these centres are susceptible to attack by the reagents. These electron displacements occur through inductive electromeric, resonance and hyperconjugation effects. Whereas inductive effect involves displacement of sigam -electrons towards the substituent, resonance effect involves delocalization of pi- electrons transmitted through the chain and both are permanent effect. Electromeric effect is the complete transfer of a shared pair of pi - electrons to one of the atoms joined by a multiple bond on the demand of an attacking reagent. Hyperconjugation effects on the other hand involve delocalization of sigma -electrons of C-H bond of an alkyl group directly attached to an atom of unsaturated system (i.e., sigma-pi -conjugation). Both inductive and hyperconjugation effects can be used to explain the stability of carbocations and free radicals which follow the stability order : 3^(@)gt2^(@)gt1^(@) . The stability or carbanions, however, follows the reverse order. An organic reaction occurs through making and breaking of bonds. The breaking of a covalent bond may occur either homolytic leading to the formation of free radicals or heterolytic forming positively (carbocations) or negatively (carbanions) charged species. Most of the attacking reagents carry either a positive or a negative charge. The positively charged species with electron deficient centre or neutral species (free radicals, carbenes, nitrene) are collectively called electrophiles, while negatively charged species with electron rich centre or neutral species (like water, alcohol, ammonia, etc.) are called nucleophiles. Consider the following alkenes and what is correct decreasing order of stability? {:(underset("(I)")underset("But-1-ene")(CH_(3)CH_(2)CH=CH_(2))", "underset("(II)")underset("2,3-Dimethylbut-2-ene")((CH_(3))_(2)C=(CH_(3))_(2))","),(underset("(III)")underset("2-Methylbut-2-ene")((CH_(3))_(2)C=CHCH_(3))", "underset("(IV)")underset("2-Methylpropene")((CH_(3))_(2)C=CH_(3))):}

The electronic displacements in covalent bonds may occur either in the ground state under the influence of an atom or a substituent group or in presence of an appropriate attacking reagent. As a result of these electron displacements, centres of different electron densities are created and these centres are susceptible to attack by the reagents. These electron displacements occur through inductive electromeric, resonance and hyperconjugation effects. Whereas inductive effect involves displacement of sigma -electrons towards the substituent, resonance effect involves delocalization of pi- electrons transmitted through the chain and both are permanent effect. Electromeric effect is the complete transfer of a shared pair of pi - electrons to one of the atoms joined by a multiple bond on the demand of an attacking reagent. Hyperconjugation effects on the other hand involve delocalization of sigma -electrons of C-H bond of an alkyl group directly attached to an atom of unsaturated system (i.e., sigma-pi -conjugation). Both inductive and hyperconjugation effects can be used to explain the stability of carbocations and free radicals which follow the stability order : 3^(@)gt2^(@)gt1^(@) . The stability or carbanions, however, follows the reverse order. An organic reaction occurs through making and breaking of bonds. The breaking of a covalent bond may occur either homolytic leading to the formation of free radicals or heterolytic forming positively (carbocations) or negatively (carbanions) charged species. Most of the attacking reagents carry either a positive or a negative charge. The positively charged species with electron deficient centre or neutral species (free radicals, carbenes, nitrene) are collectively called electrophiles, while negatively charged species with electron rich centre or neutral species (like water, alcohol, ammonia, etc.) are called nucleophiles. Which of the following is most stable cation?